100050 : AARSKOG SYNDROME 100070 : ABDOMINAL AORTIC ANEURYSM 100100 : ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY AND CRYPTORCHIDISM 100200 : ABDUCENS PALSY *100300 : ABSENCE DEFECT OF LIMBS, SCALP, AND SKULL *100500 : ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER *100600 : ACANTHOSIS NIGRICANS *100640 : ALDEHYDE DEHYDROGENASE 1 FAMILY, MEMBER A1; ALDH1A1 *100650 : ALDEHYDE DEHYDROGENASE 2 FAMILY; ALDH2 *100660 : ALDEHYDE DEHYDROGENASE, FAMILY 3, SUBFAMILY A, MEMBER 1; ALDH3A1 *100670 : ALDEHYDE DEHYDROGENASE 1 FAMILY, MEMBER B1; ALDH1B1 100675 : ACETAMINOPHEN METABOLISM *100678 : ACETYL-CoA ACETYLTRANSFERASE 2; ACAT2 100680 : ACETYLCHOLINESTERASE EXPRESSION; ACEE *100690 : CHOLINERGIC RECEPTOR, NICOTINIC, ALPHA POLYPEPTIDE 1; CHRNA1 100700 : ACHARD SYNDROME *100710 : CHOLINERGIC RECEPTOR, NICOTINIC, BETA POLYPEPTIDE 1; CHRNB1 *100720 : CHOLINERGIC RECEPTOR, NICOTINIC, DELTA POLYPEPTIDE; CHRND *100725 : CHOLINERGIC RECEPTOR, NICOTINIC, EPSILON POLYPEPTIDE; CHRNE *100730 : CHOLINERGIC RECEPTOR, NICOTINIC, GAMMA POLYPEPTIDE; CHRNG ^100735 : MOVED TO 142445 *100740 : ACETYLCHOLINESTERASE; ACHE *100790 : ACHAETE-SCUTE COMPLEX, DROSOPHILA, HOMOLOG-LIKE 1; ASCL1 #100800 : ACHONDROPLASIA; ACH *100820 : ACHOO SYNDROME *100850 : ACONITASE, MITOCHONDRIAL; ACO2 *100880 : ACONITASE, SOLUBLE; ACO1 *100900 : ACONITATE HYDRATASE, SOLUBLE *101000 : NEUROFIBROMATOSIS, TYPE II; NF2 101120 : ACROCEPHALOPOLYSYNDACTYLY TYPE III #101200 : APERT SYNDROME #101400 : SAETHRE-CHOTZEN SYNDROME; SCS #101600 : PFEIFFER SYNDROME *101800 : ACRODYSOSTOSIS 101805 : ACROFACIAL DYSOSTOSIS, CATANIA TYPE 101840 : ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT *101850 : ACROKERATOELASTOIDOSIS; AKE *101900 : ACROKERATOSIS VERRUCIFORMIS 102000 : ACROLEUKOPATHY, SYMMETRIC *102100 : ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA *102150 : ACROMEGALOID FACIAL APPEARANCE SYNDROME *102200 : ACROMEGALY *102300 : ACROMELALGIA, HEREDITARY *102350 : ACROMIAL DIMPLES 102370 : ACROMICRIC DYSPLASIA 102400 : ACROOSTEOLYSIS *102480 : ACROSIN; ACR 102490 : ACRORENOOCULAR SYNDROME *102500 : ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE *102510 : ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF 102520 : ACRORENAL SYNDROME *102525 : ACROSOMAL VESICLE PROTEIN 1; ACRV1 102530 : ACROSOME MALFORMATION OF SPERMATOZOA *102540 : ACTIN, ALPHA, CARDIAC MUSCLE; ACTC *102545 : ACTIN, GAMMA-2, SMOOTH MUSCLE, ENTERIC; ACTG2 ^102550 : MOVED TO 102630 *102560 : ACTIN, GAMMA-1; ACTG1 *102565 : FILAMIN C; FLNC *102570 : ACTIN, PLATELET *102573 : ACTININ, ALPHA-2; ACTN2 *102574 : ACTININ, ALPHA-3; ACTN3 *102575 : ACTININ, ALPHA-1; ACTN1 *102576 : ACTIVIN A RECEPTOR, TYPE I; ACVR1 *102577 : ACTIVATOR 1, 37-KD SUBUNIT; RFC4 *102578 : ACUTE PROMYELOCYTIC LEUKEMIA, INDUCER OF; PML *102579 : REPLICATION FACTOR C, 140-KD SUBUNIT; RFC1 *102581 : ACTIVIN A RECEPTOR, TYPE II; ACVR2 *102582 : SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 3; STAT3 102590 : ACYLASE, COBALT-ACTIVATED *102593 : ACYLOXYACYL HYDROLASE; AOAH *102595 : ACYLPHOSPHATASE 2, MUSCLE TYPE; ACYP2 *102600 : ADENINE PHOSPHORIBOSYLTRANSFERASE; APRT *102610 : ACTIN, ALPHA, SKELETAL MUSCLE 1; ACTA1 *102620 : ACTIN, ALPHA, SMOOTH MUSCLE, AORTIC; ACTSA *102630 : ACTIN, BETA; ACTB ^102640 : MOVED TO 102630 *102642 : STEROL O-ACYLTRANSFERASE; SOAT *102645 : ACYLPEPTIDE HYDROLASE; APH 102650 : ADACTYLIA, UNILATERAL 102660 : ADAMANTINOMA OF LONG BONES *102670 : MUCOSAL VASCULAR ADDRESSIN CELL ADHESION MOLECULE 1; MADCAM1 *102680 : ADDUCIN 1; ADD1 *102681 : ADDUCIN 2; ADD2 102699 : ADENO-ASSOCIATED VIRUS INTEGRATION SITE 1; AAVS1 *102700 : ADENOSINE DEAMINASE; ADA 102710 : ADENOSINE DEAMINASE COMPLEXING PROTEIN 1; ADCP1 *102720 : DIPEPTIDYL PEPTIDASE IV; DPP4 102730 : ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO *102750 : ADENOSINE KINASE; ADK *102770 : ADENOSINE MONOPHOSPHATE DEAMINASE 1; AMPD1 *102771 : ADENOSINE MONOPHOSPHATE DEAMINASE 2; AMPD2 *102772 : ADENOSINE MONOPHOSPHATE DEAMINASE 3; AMPD3 *102775 : ADENOSINE A1 RECEPTOR; ADORA1 *102776 : ADENOSINE A2 RECEPTOR; ADORA2A *102777 : ADENOSINE A2 RECEPTOR-LIKE; ADORA2L1 *102800 : ADENOSINE TRIPHOSPHATASE DEFICIENCY, ANEMIA DUE TO #102900 : ADENOSINE TRIPHOSPHATE, ELEVATED, OF ERYTHROCYTES *102910 : ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL F1 COMPLEX, BETA SUBUNIT; ATP5B ^102920 : REMOVED FROM DATABASE ^102930 : REMOVED FROM DATABASE ^102940 : REMOVED FROM DATABASE ^102970 : REMOVED FROM DATABASE *102980 : ADENYLATE CYCLASE-ACTIVATING POLYPEPTIDE 1; ADCYAP1 *102981 : ADENYLATE CYCLASE-ACTIVATING POLYPEPTIDE 1, RECEPTOR FOR; ADCYAP1R1 102990 : ADENYLATE KINASE, MUSCLE, DEFICIENCY OF *103000 : ADENYLATE KINASE 1; AK1 *103020 : ADENYLATE KINASE 2; AK2 *103030 : ADENYLATE KINASE 3; AK3 *103050 : ADENYLOSUCCINATE LYASE; ADSL *103060 : ADENYLOSUCCINATE SYNTHETASE; ADSS *103070 : ADENYLATE CYCLASE 8; ADCY8 *103071 : ADENYLATE CYCLASE 2; ADCY2 *103072 : ADENYLATE CYCLASE 1; ADCY1 103100 : ADIE SYNDROME *103180 : ADP-RIBOSYLATION FACTOR 1; ARF1 *103188 : ADP-RIBOSYLATION FACTOR 5; ARF5 *103190 : ADP-RIBOSYLATION FACTOR 3; ARF3 *103195 : ADIPOSE DIFFERENTIATION-RELATED PROTEIN; ADRP 103200 : ADIPOSIS DOLOROSA *103220 : SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER), MEMBER 4; SLC25A4 103230 : ADRENOCORTICAL HYPOFUNCTION, CHRONIC PRIMARY CONGENITAL *103260 : ADRENODOXIN; ADX *103270 : ADRENODOXIN REDUCTASE; ADXR *103275 : ADRENOMEDULLIN; ADM *103280 : H19 GENE; H19 #103285 : ADULT SYNDROME 103300 : AGLOSSIA-ADACTYLIA *103320 : AGRIN; AGRN ^103321 : MOVED TO 128239 *103390 : AHNAK NUCLEOPROTEIN 103400 : AINHUM *103420 : ALACRIMA, CONGENITAL #103470 : ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS #103500 : TIETZ SYNDROME #103580 : ALBRIGHT HEREDITARY OSTEODYSTROPHY; AHO 103581 : ALBRIGHT HEREDITARY OSTEODYSTROPHY 2; AHO2 *103600 : ALBUMIN; ALB *103700 : ALCOHOL DEHYDROGENASE 1A, ALPHA POLYPEPTIDE; ADH1 *103710 : ALCOHOL DEHYDROGENASE 5, CHI POLYPEPTIDE; ADH5 *103720 : ALCOHOL DEHYDROGENASE 1B, BETA POLYPEPTIDE; ADH2 *103730 : ALCOHOL DEHYDROGENASE 1C, GAMMA POLYPEPTIDE; ADH3 *103735 : ALCOHOL DEHYDROGENASE 6; ADH6 *103740 : ALCOHOL DEHYDROGENASE 4; ADH4 #103780 : ALCOHOLISM *103800 : ALDER ANOMALY *103830 : ALDO-KETO REDUCTASE FAMILY 1, MEMBER A1; AKR1A1 *103850 : ALDOLASE A, FRUCTOSE-BISPHOSPHATE; ALDOA *103870 : ALDOLASE C, FRUCTOSE-BISPHOSPHATE; ALDOC *103880 : ALDO-KETO REDUCTASE FAMILY 1, MEMBER B1; AKR1B1 *103890 : ALDOSE REDUCTASE M; ARM #103900 : HYPERALDOSTERONISM, FAMILIAL, TYPE I 103920 : ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS *103950 : ALPHA-2-MACROGLOBULIN; A2M 104000 : ALOPECIA AREATA 104100 : ALOPECIA CONGENITA WITH KERATOSIS PALMOPLANTARIS 104110 : ALOPECIA, FAMILIAL FOCAL *104130 : ALOPECIA, PSYCHOMOTOR EPILEPSY, PYORRHEA, AND MENTAL SUBNORMALITY *104145 : AFAMIN; AFM *104150 : ALPHA-FETOPROTEIN; AFP *104155 : ALPHA-FETOPROTEIN ENHANCER-BINDING PROTEIN *104160 : ALPHA-GLUCOSIDASE, NEUTRAL, AB FORM; GANAB *104170 : ALPHA-GALACTOSIDASE B; GALB *104175 : GLYCOPROTEIN ALPHA-GALACTOSYLTRANSFERASE 1; GGTA1 *104180 : ALPHA-GLUCOSIDASE C, NEUTRAL; GANC *104200 : ALPORT SYNDROME, AUTOSOMAL DOMINANT *104210 : ALPHA-2A-ADRENERGIC RECEPTOR; ADRA2A *104219 : ALPHA-1D-ADRENERGIC RECEPTOR; ADRA1D *104220 : ALPHA-1B-ADRENERGIC RECEPTOR; ADRA1B *104221 : ALPHA-1A-ADRENERGIC RECEPTOR; ADRA1A ^104222 : MOVED TO 104219 *104225 : LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN-ASSOCIATED PROTEIN 1; LRPAP1 *104230 : FUCOSYLTRANSFERASE 4; FUT4 *104240 : SIALYLTRANSFERASE 4C; SIAT4C *104250 : ALPHA-2C-ADRENERGIC RECEPTOR; ADRA2C *104260 : ALPHA-2B-ADRENERGIC RECEPTOR; ADRA2B 104290 : ALTERNATING HEMIPLEGIA OF CHILDHOOD #104300 : ALZHEIMER DISEASE; AD #104310 : ALZHEIMER DISEASE 2; AD2 *104311 : ALZHEIMER DISEASE, FAMILIAL, TYPE 3 104350 : AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM 104400 : AMELIA AND TERMINAL TRANSVERSE HEMIMELIA #104500 : AMELOGENESIS IMPERFECTA 2, HYPOPLASTIC LOCAL, AUTOSOMAL DOMINANT; AIH2 *104510 : AMELOGENESIS IMPERFECTA, HYPOMATURATION-HYPOPLASIC TYPE, WITH TAURODONTISM; AIHHT *104530 : AMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE *104570 : AMELOONYCHOHYPOHIDROTIC SYNDROME 104600 : AMENORRHEA-GALACTORRHEA SYNDROME *104610 : AMILORIDE-BINDING PROTEIN 1; ABP1 *104613 : CHAPERONIN CONTAINING T-COMPLEX POLYPEPTIDE 1, SUBUNIT 6A; CCT6A *104614 : SOLUTE CARRIER FAMILY 3 (CYSTINE, DIBASIC, AND NEUTRAL AMINO ACID TRANSPORTER), MEMBER 1; SLC3A1 *104615 : SOLUTE CARRIER FAMILY 7, MEMBER 1; SLC7A1 *104620 : AMINOACYLASE 1; ACY1 *104640 : AMPHIREGULIN; AREG *104650 : AMYLASE, PANCREATIC, A; AMY2A *104660 : AMYLASE, PANCREATIC, B; AMY2B *104700 : AMYLASE, SALIVARY; AMY1 *104701 : AMYLASE, SALIVARY, B; AMY1B *104702 : AMYLASE, SALIVARY, C; AMY1C *104740 : AMYLOID BETA A4 PRECURSOR PROTEIN-LIKE 1; APPL1 *104750 : SERUM AMYLOID A1; SAA1 *104751 : SERUM AMYLOID A2; SAA2 *104752 : SERUM AMYLOID A4; SAA4 *104760 : AMYLOID BETA A4 PRECURSOR PROTEIN; APP *104770 : AMYLOID P COMPONENT, SERUM; APCS *104775 : AMYLOID BETA A4 PRECURSOR-LIKE PROTEIN 1; APLP1 *104776 : AMYLOID BETA A4 PRECURSOR-LIKE PROTEIN 2; APLP2 #105120 : AMYLOIDOSIS V #105150 : AMYLOIDOSIS VI #105200 : AMYLOIDOSIS, FAMILIAL VISCERAL *105210 : AMYLOIDOSIS VII *105250 : AMYLOIDOSIS, PRIMARY CUTANEOUS 105300 : AMYOTROPHIC DYSTONIC PARAPLEGIA #105400 : AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1 105500 : AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX OF GUAM *105550 : AMYOTROPHIC LATERAL SCLEROSIS WITH FRONTOTEMPORAL DEMENTIA 105563 : ANAL SPHINCTER DYSPLASIA; ASDP 105565 : ANAL SPHINCTER MYOPATHY, INTERNAL 105570 : ANDROSTENONE, ABILITY TO SMELL 105580 : ANAL CANAL CARCINOMA *105590 : ANAPLASTIC LYMPHOMA KINASE; ALK *105600 : ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE III; CDAN3 #105650 : DIAMOND-BLACKFAN ANEMIA, AUTOSOMAL DOMINANT *105800 : ANEURYSM, INTRACRANIAL BERRY 105805 : ANEURYSM OF INTERVENTRICULAR SEPTUM #105830 : ANGELMAN SYNDROME; AS 105835 : ANGEL-SHAPED PHALANGOEPIPHYSEAL DYSPLASIA; ASPED *105850 : ANGIOGENIN; ANG 106050 : ANGIOMA SERPIGINOSUM *106070 : ANGIOMA, HEREDITARY NEUROCUTANEOUS #106100 : ANGIOEDEMA, HEREDITARY; HAE *106150 : ANGIOTENSIN I; AGT 106160 : ANGIOTENSIN II BINDING PROTEIN *106165 : ANGIOTENSIN RECEPTOR 1; AGTR1 *106180 : ANGIOTENSIN I-CONVERTING ENZYME; ACE 106190 : ANHIDROSIS, FAMILIAL GENERALIZED, WITH NORMAL SWEAT GLANDS *106195 : SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 3; SLC4A3 #106200 : ANIRIDIA; AN1 *106210 : PAIRED BOX GENE 6; PAX6 106220 : ANIRIDIA AND ABSENT PATELLA 106230 : ANIRIDIA, MICROCORNEA, AND SPONTANEOUSLY REABSORBED CATARACT 106240 : ANISOCORIA 106250 : ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT PALATE #106260 : ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE 106280 : ANKYLOGLOSSIA *106300 : ANKYLOSING SPONDYLITIS; AS 106400 : ANKYLOSING VERTEBRAL HYPEROSTOSIS WITH TYLOSIS *106410 : ANKYRIN 2; ANK2 *106490 : ANNEXIN A3; ANXA3 *106491 : ANNEXIN A4; ANXA4 106500 : ANNULAR ERYTHEMA #106600 : HYPODONTIA, AUTOSOMAL DOMINANT; HYD1 *106700 : TOTAL ANOMALOUS PULMONARY VENOUS RETURN; TAPVR1 106750 : ANONYCHIA WITH FLEXURAL PIGMENTATION 106900 : ANONYCHIA-ECTRODACTYLY 106990 : ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY *106995 : ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES 107000 : ANONYCHIA-ONYCHODYSTROPHY *107100 : ANORECTAL ANOMALIES 107200 : ANOSMIA, CONGENITAL *107240 : ANTIGEN MSK39 IDENTIFIED BY MONOCLONAL ANTIBODY 5.1H11; MSK39 #107250 : ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS; ASMD *107253 : ANTIGEN MDF1 IDENTIFIED BY MONOCLONAL ANTIBODY A-3A4; MDF1 *107254 : ANTIGEN IDENTIFIED BY MONOCLONAL ANTIBODY 30.2A8; MIC12 *107257 : ANTIGEN MSK3 IDENTIFIED BY MONOCLONAL ANTIBODY M68; MSK3 *107260 : ANTIGEN MSK41 IDENTIFIED BY MONOCLONAL ANTIBODY E3; MSK41 *107265 : CD19 ANTIGEN; CD19 *107266 : CD22 ANTIGEN; CD22 *107269 : CD44 ANTIGEN; CD44 *107270 : CD38 ANTIGEN; CD38 *107271 : CD59 ANTIGEN P18-20; CD59 *107272 : CD72 ANTIGEN; CD72 *107273 : CD69 ANTIGEN; CD69 *107280 : ALPHA-1-ANTICHYMOTRYPSIN; AACT *107285 : SECRETORY LEUKOCYTE PROTEASE INHIBITOR; SLPI *107290 : ANTIPYRINE METABOLISM *107300 : ANTITHROMBIN III DEFICIENCY *107310 : SOLUTE CARRIER FAMILY 9, ISOFORM A1; SLC9A1 107320 : ANTIPHOSPHOLIPID SYNDROME *107323 : ALDEHYDE DEHYDROGENASE 7 FAMILY, MEMBER A1; ALDH7A1 *107325 : ANTISENSE ERCC1; ASE1 *107400 : PROTEASE INHIBITOR 1; PI *107410 : PROTEASE INHIBITOR 1-LIKE; PIL 107440 : ANTIVIRAL STATE REPRESSOR, REGULATOR OF; AVRR *107450 : INTERFERON, ALPHA, BETA, AND OMEGA, RECEPTOR 1; IFNAR1 ^107460 : MOVED TO 107450 *107470 : INTERFERON, GAMMA, RECEPTOR 1; IFNGR1 #107480 : TOWNES-BROCKS SYNDROME; TBS 107500 : AORTIC ARCH ANOMALY WITH PECULIAR FACIES AND MENTAL RETARDATION 107550 : AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA *107580 : TRANSCRIPTION FACTOR AP2-ALPHA; TFAP2A *107600 : APLASIA CUTIS CONGENITA 107601 : APLASIA CUTIS CONGENITA AND COARCTATION OF AORTA; ACCCA 107640 : APNEA, CENTRAL SLEEP *107650 : APNEA, OBSTRUCTIVE SLEEP *107670 : APOLIPOPROTEIN A-II; APOA2 *107680 : APOLIPOPROTEIN A-I; APOA1 *107690 : APOLIPOPROTEIN A-IV; APOA4 107700 : APPENDICITIS, PRONENESS TO *107710 : APOLIPOPROTEIN C-I; APOC1 *107720 : APOLIPOPROTEIN C-III; APOC3 *107730 : APOLIPOPROTEIN B; APOB *107740 : APOLIPOPROTEIN D; APOD *107741 : APOLIPOPROTEIN E; APOE *107748 : APEX NUCLEASE; APEX #107750 : ARBITRARY RESTRICTION POLYMORPHISM 1 107760 : APOLIPOPROTEIN F; APOF *107770 : LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 1; LRP1 *107773 : NUCLEAR RECEPTOR SUBFAMILY 2, GROUP F, MEMBER 2; NR2F2 *107776 : AQUAPORIN 1; AQP1 *107777 : AQUAPORIN 2; AQP2 107800 : ARCUS CORNEAE *107820 : ARGINYL-tRNA SYNTHETASE; RARS *107830 : ARGINASE II; ARG2 ^107840 : MOVED TO 215700 107850 : ARM FOLDING PREFERENCE 107900 : ARMS, MALFORMATION OF *107910 : CYTOCHROME P450, SUBFAMILY XIX; CYP19 107920 : AROMATIC ALPHA-KETO ACID REDUCTASE *107930 : AROMATIC L-AMINO ACID DECARBOXYLASE; AADC *107940 : ARRESTIN, BETA, 1; ARRB1 *107941 : ARRESTIN, BETA, 2; ARRB2 *107950 : ARRHENOBLASTOMA--THYROID ADENOMA *107970 : ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1 108000 : ARTERIES, ANOMALIES OF #108010 : ARTERIOVENOUS MALFORMATIONS OF THE BRAIN 108050 : ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS 108100 : ARTHRITIS, SACROILIAC 108110 : ARTHROGRYPOSIS MULTIPLEX CONGENITA; AMC *108120 : ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE 1; AMCD1 108130 : ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE II 108140 : ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE II, WITH CRANIOFACIAL ABNORMALITIES 108145 : ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES 108200 : ARTHROGRYPOSIS-LIKE HAND ANOMALY AND SENSORINEURAL DEAFNESS #108300 : STICKLER SYNDROME, TYPE I; STL1 108320 : ARTICHOKE, MODIFICATION OF TASTE BY *108330 : CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 1; CYP1A1 #108340 : ARYL HYDROCARBON HYDROXYLASE INDUCIBILITY *108345 : N-ACETYLTRANSFERASE 1; NAT1 *108355 : GROWTH FACTOR RECEPTOR-BOUND PROTEIN 2; GRB2 *108360 : ASIALOGLYCOPROTEIN RECEPTOR 1; ASGR1 *108361 : ASIALOGLYCOPROTEIN RECEPTOR 2; ASGR2 *108370 : ASPARAGINE SYNTHETASE; ASNS 108390 : ASPARAGUS, SPECIFIC SMELL HYPERSENSITIVITY ^108400 : REMOVED FROM DATABASE *108410 : ASPARAGINYL-tRNA SYNTHETASE; NARS 108420 : ASPERMIOGENESIS FACTOR; ASG 108450 : ASYMMETRIC SHORT STATURE SYNDROME #108500 : EPISODIC ATAXIA, TYPE 2; EA2 *108600 : ATAXIA, SPASTIC, AUTOSOMAL DOMINANT; SAX1 *108650 : ATAXIA, SPASTIC, WITH CONGENITAL MIOSIS 108700 : ATAXIA WITH FASCICULATIONS 108720 : ATELOSTEOGENESIS, TYPE I *108721 : ATELOSTEOGENESIS, TYPE III 108725 : ATHEROSCLEROSIS SUSCEPTIBILITY; ATHS *108728 : ATP CITRATE LYASE; ACLY *108729 : ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL F1 COMPLEX, GAMMA SUBUNIT 1; ATP5C1 *108730 : ATPase, Ca(2+)-TRANSPORTING, FAST-TWITCH 1; ATP2A1 *108731 : ATPase, Ca(2+)-TRANSPORTING, PLASMA MEMBRANE, 1; ATP2B1 *108732 : ATPase, Ca(2+)-TRANSPORTING, PLASMA MEMBRANE, 4; ATP2B4 *108733 : ATPase, Ca(2+)-TRANSPORTING, PLASMA MEMBRANE, 2; ATP2B2 *108740 : ATPase, Ca(2+)-TRANSPORTING, SLOW-TWITCH; ATP2A2 *108745 : ATPase, H+ TRANSPORTING, LYSOSOMAL; ATP6L *108746 : ATPase, H+ TRANSPORTING, LYSOSOMAL, 31-KD, V1 SUBUNIT E; ATP6V1E *108760 : ATRESIA OF EXTERNAL AUDITORY CANAL AND CONDUCTION DEAFNESS 108770 : ATRIAL CARDIOMYOPATHY WITH HEART BLOCK *108780 : NATRIURETIC PEPTIDE PRECURSOR A; NPPA *108800 : ATRIAL SEPTAL DEFECT; ASD #108900 : ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS 108950 : ATRIAL TACHYARRHYTHMIA WITH SHORT PR INTERVAL *108960 : NATRIURETIC PEPTIDE RECEPTOR A/GUANYLATE CYCLASE A; NPR1 *108961 : NATRIURETIC PEPTIDE RECEPTOR B/GUANYLATE CYCLASE B; NPR2 *108962 : NATRIURETIC PEPTIDE RECEPTOR C; NPR3 108970 : ATRIOPEPTIDASE 108980 : ATRIOVENTRICULAR CONDUCTION TIME *108985 : ATROPHIA AREATA; AA *108990 : ATTACHED CELL ANTIGEN 28.3.7; MIC7 *109000 : AURICULOOSTEODYSPLASIA 109050 : AUROCEPHALOSYNDACTYLY *109090 : SJOGREN SYNDROME ANTIGEN B; SSB *109091 : CALRETICULIN; CALR *109092 : SJOGREN SYNDROME ANTIGEN A1; SSA1 #109100 : AUTOIMMUNE DISEASES *109110 : AUTONOMOUSLY REPLICATING SEQUENCE 1 109120 : AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES 109130 : AXIAL OSTEOMALACIA *109135 : AXL RECEPTOR TYROSINE KINASE; AXL #109150 : MACHADO-JOSEPH DISEASE; MJD *109160 : AZOTEMIA, FAMILIAL *109170 : LYMPHOCYTE ANTIGEN 117; LY117 109180 : BABOON M7 VIRUS INTEGRATION SITE; BEVI *109190 : SOLUTE CARRIER FAMILY 1 (NEUTRAL AMINO ACID TRANSPORTER), MEMBER 5; SLC1A5 *109195 : BACTERICIDAL PERMEABILITY-INCREASING PROTEIN; BPI *109200 : ALOPECIA, ANDROGENETIC *109270 : SOLUTE CARRIER FAMILY 4, ANION EXCHANGER, MEMBER 1; SLC4A1 *109280 : SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 2; SLC4A2 109300 : BANKI SYNDROME *109350 : GASTROESOPHAGEAL REFLUX 109390 : BASAL CELL CARCINOMAS WITH MILIA AND COARSE, SPARSE HAIR #109400 : BASAL CELL NEVUS SYNDROME; BCNS *109480 : BASIGIN; BSG 109500 : BASILAR IMPRESSION, PRIMARY *109530 : CD48 ANTIGEN; CD48 *109535 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 5; TNFRSF5 109540 : B-CELL GROWTH FACTOR; BCGF *109543 : B-CELL MALIGNANCY, LOW-GRADE *109545 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 17; TNFRSF17 *109560 : B-CELL LEUKEMIA/LYMPHOMA 3; BCL3 *109565 : B-CELL LYMPHOMA 6; BCL6 *109580 : B-CELL TRANSLOCATION GENE 1; BTG1 109600 : BEETURIA *109610 : BENZODIAZEPINE RECEPTOR, PERIPHERAL TYPE; BZRP *109630 : BETA-1-ADRENERGIC RECEPTOR; ADRB1 *109635 : BETA-ADRENERGIC RECEPTOR KINASE 1; ADRBK1 *109636 : BETA-ADRENERGIC RECEPTOR KINASE 2; ADRBK2 *109640 : BETA-GLYCEROL PHOSPHATASE; GPB 109650 : BEHCET SYNDROME *109660 : BETA-AMINO ACIDS, RENAL TRANSPORT OF; AABT 109670 : BETA-ADRENERGIC STIMULATION, RESPONSE TO; BAS *109675 : SIALYLTRANSFERASE 1; SIAT1 *109684 : 17-@BETA-HYDROXYSTEROID DEHYDROGENASE I; HSD17B1 *109685 : 17-@BETA-HYDROXYSTEROID DEHYDROGENASE II; HSD17B2 *109690 : BETA-2-ADRENERGIC RECEPTOR; ADRB2 *109691 : BETA-3-ADRENERGIC RECEPTOR; ADRB3 *109700 : BETA-2-MICROGLOBULIN; B2M *109710 : BETA-2-MICROGLOBULIN REGULATOR; B2MR *109715 : 3-@BETA-HYDROXYSTEROID DEHYDROGENASE/DELTA-ISOMERASE, TYPE I 109720 : BILIARY CIRRHOSIS, PRIMARY; PBC 109730 : BICUSPID AORTIC VALVE 109740 : BIFID NOSE *109750 : BILIVERDIN REDUCTASE A; BLVRA *109760 : 5-@HYDROXYTRYPTAMINE RECEPTOR 1A; HTR1A *109770 : CARCINOEMBRYONIC ANTIGEN-RELATED CELL ADHESION MOLECULE 1; CEACAM1 *109780 : BKM DNA #109800 : BLADDER CANCER 109820 : BLADDER DIVERTICULUM 109900 : BLEPHAROCHALASIS AND DOUBLE LIP 110000 : BLEPHAROCHALASIS, SUPERIOR 110050 : BLEPHARONASOFACIAL MALFORMATION SYNDROME #110100 : BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES 110150 : BLEPHAROPTOSIS, MYOPIA, AND ECTOPIA LENTIS 110250 : BLOOD GROUP--ABO SUPPRESSOR *110300 : ABO BLOOD GROUP; ABO 110310 : BLOOD GROUP--ABH ANTIGEN, TYPE 2 *110350 : BLOOD GROUP--AHONEN; AN #110450 : BLOOD GROUP--COLTON; CO #110500 : BLOOD GROUP--DIEGO SYSTEM; DI #110600 : BLOOD GROUP--DOMBROCK SYSTEM; DO *110700 : BLOOD GROUP--DUFFY SYSTEM; FY 110720 : BLOOD GROUP--En *110750 : BLOOD GROUP--GERBICH; Ge #110800 : BLOOD GROUP--I SYSTEM; Ii *110900 : BLOOD GROUP--KELL-CELLANO SYSTEM; KEL *111000 : BLOOD GROUP--KIDD SYSTEM; JK *111100 : FUCOSYLTRANSFERASE 3; FUT3 *111130 : BLOOD GROUP--LKE; LKE *111150 : BLOOD GROUP--LUTHERAN INHIBITOR *111200 : BLOOD GROUP--LUTHERAN SYSTEM; LU *111250 : LANDSTEINER-WIENER BLOOD GROUP; LW *111300 : BLOOD GROUP--MN LOCUS; MN 111360 : BLOOD GROUP--NEWFOUNDLAND; NFLD #111380 : BLOOD GROUP--OK; OK *111400 : BLOOD GROUP--P SYSTEM *111410 : BLOOD GROUP--P SYSTEM, SECOND LOCUS #111500 : BLOOD GROUP--PRIVATE SYSTEMS #111600 : BLOOD GROUP--PUBLIC SYSTEMS 111620 : BLOOD GROUP--RADIN ANTIGEN; Rd *111680 : RHESUS BLOOD GROUP, D ANTIGEN; RHD #111690 : BLOOD GROUP--RHESUS SYSTEM E POLYPEPTIDE; RHE *111700 : RHESUS BLOOD GROUP, CcEe ANTIGENS; RHCE *111730 : N-ACETYLGALACTOSAMINYLTRANSFERASE II *111740 : BLOOD GROUP--Ss LOCUS; Ss *111750 : BLOOD GROUP--SCIANNA SYSTEM; Sc *111800 : BLOOD GROUP--STOLTZFUS SYSTEM; Sf *112000 : BLOOD GROUP--Ul SYSTEM; UL #112010 : BLOOD GROUP--WALDNER TYPE; WD #112050 : BLOOD GROUP--WRIGHT ANTIGEN; Wr #112100 : BLOOD GROUP--Yt SYSTEM; YT *112200 : BLUE RUBBER BLEB NEVUS *112203 : CD80 ANTIGEN; CD80 *112205 : CD79A ANTIGEN; CD79A *112210 : MEMBRANE-SPANNING 4 DOMAINS, SUBFAMILY A, MEMBER 1; MS4A1 112240 : BONE FRAGILITY WITH CRANIOSYNOSTOSIS, OCULAR PROPTOSIS, HYDROCEPHALUS, AND DISTINCTIVE FACIAL FEATURES *112250 : DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA *112260 : GAMMA-CARBOXYGLUTAMIC ACID PROTEIN, BONE; BGLAP *112261 : BONE MORPHOGENETIC PROTEIN 2; BMP2 *112262 : BONE MORPHOGENETIC PROTEIN 4; BMP4 *112263 : BONE MORPHOGENETIC PROTEIN 3; BMP3 *112264 : BONE MORPHOGENETIC PROTEIN 1; BMP1 *112265 : BONE MORPHOGENETIC PROTEIN 5; BMP5 *112266 : BONE MORPHOGENETIC PROTEIN 6; BMP6 *112267 : BONE MORPHOGENETIC PROTEIN 7; BMP7 112270 : BONE PAIN, PERIODIC *112300 : BOOK SYNDROME 112310 : BOOMERANG DYSPLASIA 112350 : BOWING OF LEGS, ANTERIOR, WITH DWARFISM 112370 : BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUS ADDUCTUS, AND DEVELOPMENTAL DELAY *112410 : HYPERTENSION WITH BRACHYDACTYLY 112430 : BRACHYDACTYLY, LONG-THUMB TYPE 112440 : BRACHYDACTYLY, COMBINED B AND E TYPES 112450 : BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION #112500 : BRACHYDACTYLY, TYPE A1; BDA1 *112600 : BRACHYDACTYLY, TYPE A2; BDA2 *112700 : BRACHYDACTYLY, TYPE A3; BDA3 *112800 : BRACHYDACTYLY, TYPE A4; BDA4 *112900 : BRACHYDACTYLY, TYPE A5, WITH NAIL DYSPLASIA 112910 : BRACHYDACTYLY, TYPE A6; BDA6 #113000 : BRACHYDACTYLY, TYPE B1; BDB1 *113100 : BRACHYDACTYLY, TYPE C; BDC *113200 : BRACHYDACTYLY, TYPE D; BDD *113300 : BRACHYDACTYLY, TYPE E; BDE 113301 : BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II 113310 : BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA 113400 : BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA 113450 : BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME 113470 : BRACHYMESOMELIA-RENAL SYNDROME 113475 : BRACHYMETATARSUS IV 113477 : BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME 113480 : BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME 113500 : BRACHYRACHIA *113503 : BRADYKININ RECEPTOR B2; BDKRB2 *113505 : BRAIN-DERIVED NEUROTROPHIC FACTOR; BDNF *113508 : TYROSINE 3-MONOOXYGENASE/TRYPTOPHAN 5-MONOOXYGENASE ACTIVATION PROTEIN, ETA ISOFORM; YWHAH *113510 : BRAIN-SPECIFIC PROTEIN Pc-1 *113520 : BRANCHED-CHAIN AMINOTRANSFERASE 1; BCAT1 *113530 : BRANCHED-CHAIN AMINOTRANSFERASE 2; BCAT2 113600 : BRANCHIAL CLEFT ANOMALIES 113610 : BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA *113620 : BRANCHIAL CLEFTS WITH CHARACTERISTIC FACIES, GROWTH RETARDATION, IMPERFORATE NASOLACRIMAL DUCT, AND PREMATURE AGING *113630 : BREAKPOINT CLUSTER REGION-LIKE 2; BCRL2 *113640 : BREAKPOINT CLUSTER REGION-LIKE 3; BCRL3 #113650 : BRANCHIOOTORENAL DYSPLASIA *113660 : BREAKPOINT CLUSTER REGION-LIKE 4; BCRL4 113670 : BREAST, UNILATERAL GIANT 113700 : BREASTS AND NIPPLES, ABSENCE OF *113703 : RIBOSOMAL PROTEIN L13; RPL13 *113705 : BREAST CANCER, TYPE 1; BRCA1 *113710 : TREFOIL FACTOR 1; TFF1 *113720 : BREAST CANCER-ASSOCIATED DF3 ANTIGEN *113721 : BREAST CANCER-RELATED REGULATOR OF TP53 *113725 : POU DOMAIN, CLASS 4, TRANSCRIPTION FACTOR 2; POU4F2 *113730 : UNCOUPLING PROTEIN 1; UCP1 *113750 : HAIR COLOR 1; HCL1 #113800 : BULLOUS ERYTHRODERMA ICHTHYOSIFORMIS CONGENITA OF BROCQ *113810 : BULLOUS PEMPHIGOID ANTIGEN 1; BPAG1 *113811 : COLLAGEN, TYPE XVII, ALPHA-1; COL17A1 #113900 : PROGRESSIVE FAMILIAL HEART BLOCK, TYPE I; PFHBI *113950 : BUNDLE BRANCH BLOCK, FAMILIAL ISOLATED COMPLETE RIGHT *113955 : BUNGAROTOXIN, ALPHA, RECEPTOR FOR; BGTXR 113960 : BUTYRYLESTERASE 1 #113970 : BURKITT LYMPHOMA; BL *113995 : COMPLEMENT COMPONENT 5 RECEPTOR 1; C5R1 *114000 : CAFFEY DISEASE *114010 : CARBAMOYLPHOSPHATE SYNTHETASE/ASPARTATE TRANSCARBAMOYLASE/DIHYDROOROTASE; CAD *114019 : CADHERIN 15; CDH15 *114020 : CADHERIN 2; CDH2 *114021 : CADHERIN 3; CDH3 *114025 : CATENIN, ALPHA-2; CTNNA2 #114030 : CAFE-AU-LAIT SPOTS, MULTIPLE *114050 : CALBINDIN 1; CALB1 *114051 : CALBINDIN 2; CALB2 114065 : CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL *114070 : ANNEXIN A6; ANXA6 *114078 : CALCIUM/CALMODULIN-DEPENDENT PROTEIN KINASE II-ALPHA; CAMK2A *114080 : CALCIUM/CALMODULIN-DEPENDENT PROTEIN KINASE IV; CAMK4 *114085 : S100 CALCIUM-BINDING PROTEIN A10; S100A10 *114090 : CALPASTATIN; CAST 114100 : CALCIFICATION OF BASAL GANGLIA WITH OR WITHOUT HYPOCALCEMIA *114105 : PROTEIN PHOSPHATASE 3, CATALYTIC SUBUNIT, ALPHA ISOFORM; PPP3CA *114106 : PROTEIN PHOSPHATASE 3, CATALYTIC SUBUNIT, BETA ISOFORM; PPP3CB *114107 : PROTEIN PHOSPHATASE 3, CATALYTIC SUBUNIT, GAMMA ISOFORM; PPP3CC *114110 : S100 CALCIUM-BINDING PROTEIN A6; S100A6 114120 : CALCINOSIS, TUMORAL *114130 : CALCITONIN/CALCITONIN-RELATED POLYPEPTIDE, ALPHA; CALCA *114131 : CALCITONIN RECEPTOR; CALCR *114140 : CALLOSITIES, HEREDITARY PAINFUL *114150 : CAMPTOBRACHYDACTYLY *114160 : CALCITONIN-RELATED POLYPEPTIDE, BETA; CALCB *114170 : CALPAIN, SMALL SUBUNIT 1; CAPNS1 *114180 : CALMODULIN 1; CALM1 *114181 : CALMODULIN-LIKE 1; CALML1 *114182 : CALMODULIN 2; CALM2 *114183 : CALMODULIN 3; CALM3 *114184 : CALMODULIN-LIKE 3; CALML3 *114190 : CALCITONIN RECEPTOR-LIKE GENE; CALCRL *114200 : CAMPTODACTYLY *114204 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, ALPHA-2/DELTA SUBUNIT 1; CACNA2D1 *114205 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-1C SUBUNIT; CACNA1C *114206 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-1D SUBUNIT; CACNA1D *114207 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, BETA-1 SUBUNIT; CACNB1 *114208 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-1S SUBUNIT; CACNA1S *114209 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, GAMMA-1 SUBUNIT; CACNG1 *114210 : S100 CALCIUM-BINDING PROTEIN A4; S100A4 *114212 : CALCYPHOSINE; CAPS *114213 : CALDESMON 1; CALD1 *114217 : CALNEXIN; CANX *114220 : CALPAIN 1; CAPN1 *114230 : CALPAIN 2; CAPN2 *114240 : CALPAIN 3; CAPN3 *114250 : CALSEQUESTRIN 1; CASQ1 *114251 : CALSEQUESTRIN 2; CASQ2 ^114260 : MOVED TO 300006 *114280 : CAMPATH-1 ANTIGEN; CDW52 *114290 : CAMPOMELIC DYSPLASIA *114300 : CAMPTODACTYLY, CLEFT PALATE, AND CLUBFOOT *114350 : NUCLEOPORIN, 214-KD; NUP214 #114400 : LYNCH CANCER FAMILY SYNDROME II; LCFS2 114450 : CANCER, FAMILIAL, WITH IN VITRO RADIORESISTANCE #114480 : BREAST CANCER #114500 : COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS; HNPCC #114550 : HEPATOCELLULAR CARCINOMA *114580 : CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT *114600 : CANINE TEETH, ABSENCE OF UPPER PERMANENT *114610 : CANNABINOID RECEPTOR 1; CNR1 114620 : CANTU SYNDROME 114650 : CAR FACTOR DEFICIENCY 114700 : CARABELLI ANOMALY OF MAXILLARY MOLAR TEETH *114750 : CARBONIC ANHYDRASE III; CA3 *114760 : CARBONIC ANHYDRASE IV; CA4 *114761 : CARBONIC ANHYDRASE V; CA5A *114770 : CARBONIC ANHYDRASE VII; CA7 *114780 : CARBONIC ANHYDRASE VI; CA6 *114800 : CARBONIC ANHYDRASE I; CA1 *114815 : CARBONIC ANHYDRASE VIII; CA8 *114830 : CARBONYL REDUCTASE 1; CBR1 *114835 : CARBOXYLESTERASE 1; CES1 ^114836 : MOVED TO 114835 *114840 : CARBOXYL-ESTER LIPASE; CEL *114841 : CARBOXYL-ESTER LIPASE-LIKE; CELL *114850 : CARBOXYPEPTIDASE A1; CPA1 *114851 : CARBOXYPEPTIDASE A3, MAST CELL; CPA3 *114852 : CARBOXYPEPTIDASE B1, TISSUE; CPB1 *114855 : CARBOXYPEPTIDASE E; CPE *114860 : CARBOXYPEPTIDASE M; CPM *114890 : CARCINOEMBRYONIC ANTIGEN-RELATED CELL ADHESION MOLECULE 5; CEACAM5 114900 : CARCINOID TUMORS, INTESTINAL 115000 : CARDIAC ARRHYTHMIA #115080 : CARDIAC CONDUCTION DEFECT 115150 : CARDIOFACIOCUTANEOUS SYNDROME #115195 : CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2 #115196 : CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3; CMH3 #115197 : CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4 115198 : CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 5 #115200 : CARDIOMYOPATHY, DILATED, 1A; CMD1A *115210 : CARDIOMYOPATHY, FAMILIAL RESTRICTIVE 115250 : CARDIOMYOPATHY-HYPOGONADISM-COLLAGENOMA SYNDROME 115300 : CAROTENEMIA, FAMILIAL #115310 : CAROTID BODY TUMORS AND MULTIPLE EXTRAADRENAL PHEOCHROMOCYTOMAS 115400 : CARPAL DISPLACEMENT *115430 : CARPAL TUNNEL SYNDROME; CTS1 *115435 : CARTILAGE LINK PROTEIN; CRTL1 *115437 : MATRILIN 1; MATN1 *115440 : CASEIN KINASE II, ALPHA-1; CSNK2A1 *115441 : CASEIN KINASE II, BETA; CSNK2B *115442 : CASEIN KINASE II, ALPHA-2; CSNK2A2 *115450 : CASEIN, ALPHA; CSN1 *115460 : CASEIN, BETA; CSN2 #115470 : CAT EYE SYNDROME; CES *115500 : CATALASE; CAT *115501 : TYROSINASE-RELATED PROTEIN 1; TYRP1 115645 : CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION *115650 : CATARACT, ANTERIOR POLAR, 1; CTAA1 *115660 : CATARACT, CONGENITAL, CERULEAN TYPE, 1; CCA1 *115665 : CATARACT, CONGENITAL, VOLKMANN TYPE; CCV #115700 : CATARACT, CRYSTALLINE ACULEIFORM OR FROSTED *115800 : CATARACT, CRYSTALLINE CORALLIFORM *115900 : CATARACT, FLORIFORM 116100 : CATARACT, MEMBRANOUS *116150 : CATARACT-MICROCORNEA SYNDROME #116200 : CATARACT, ZONULAR PULVERULENT 1; CZP1 *116300 : CATARACT, NUCLEAR DIFFUSE NONPROGRESSIVE *116400 : CATARACT, NUCLEAR TOTAL *116600 : CATARACT, POSTERIOR POLAR 1 116700 : CATARACT, TOTAL CONGENITAL; CC *116790 : CATECHOL-O-METHYLTRANSFERASE; COMT #116800 : CATARACT, LAMELLAR *116805 : CATENIN, ALPHA-1; CTNNA1 *116806 : CATENIN, BETA-1; CTNNB1 *116810 : CATHEPSIN B; CTSB *116820 : CATHEPSIN H; CTSH *116830 : CATHEPSIN G; CTSG *116831 : GRANZYME H; GZMH *116840 : CATHEPSIN D; CTSD *116845 : CATHEPSIN S; CTSS 116850 : CATATRICHY #116860 : CEREBRAL CAVERNOUS MALFORMATIONS 1; CCM1 116870 : CELIAC ARTERY STENOSIS FROM COMPRESSION BY MEDIAN ARCUATE LIGAMENT OF DIAPHRAGM *116880 : CATHEPSIN L; CTSL *116890 : CATHEPSIN E; CTSE *116896 : CUT-LIKE, 1; CUTL1 *116897 : CCAAT/ENHANCER-BINDING PROTEIN, ALPHA; CEBPA *116898 : CCAAT/ENHANCER-BINDING PROTEIN, DELTA; CEBPD *116899 : CYCLIN-DEPENDENT KINASE INHIBITOR 1A; CDKN1A *116900 : CDC2-ASSOCIATED PROTEIN CKS1; CKS1 *116901 : CDC2-ASSOCIATED PROTEIN CKS2; CKS2 #116920 : LEUKOCYTE ADHESION DEFICIENCY, TYPE I; LAD *116930 : CELL ADHESION MOLECULE, NEURAL, 1; NCAM1 *116935 : CELL MATRIX ADHESION REGULATOR; CMAR *116940 : CELL DIVISION CYCLE 2, G1 TO S AND G2 TO M; CDC2 *116945 : MINICHROMOSOME MAINTENANCE, S. CEREVISIAE, HOMOLOG OF, 2; MCM2 *116946 : CELL DIVISION CYCLE 27; CDC27 *116947 : CELL DIVISION CYCLE 25A; CDC25A *116948 : CELL DIVISION CYCLE 34; CDC34 *116949 : CELL DIVISION CYCLE 25B; CDC25B *116950 : CELL CYCLE CONTROLLER G1 *116951 : CELL DIVISION CYCLE 2-LIKE 2; CDC2L2 *116952 : CELL DIVISION CYCLE 42; CDC42 *116953 : CYCLIN-DEPENDENT KINASE 2; CDK2 *116954 : ANTIGEN DEFINED BY MONOCLONAL ANTIBODY TRA-2-10; MIC10 *116955 : ZINC FINGER PROTEIN 9; ZNF9 *116957 : RETINOBLASTOMA-LIKE 1; RBL1 *116960 : SENESCENCE-RELATED, CELLULAR, 1; SEN1 #117000 : CENTRAL CORE DISEASE OF MUSCLE *117100 : CENTRALOPATHIC EPILEPSY *117139 : CENTROMERIC PROTEIN A; CENPA *117140 : CENTROMERIC PROTEIN B; CENPB *117141 : CENTROMERIC PROTEIN C1; CENPC1 *117142 : CENTROMERIC PROTEIN D; CENPD *117143 : CENTROMERIC PROTEIN E; CENPE ^117200 : REMOVED FROM DATABASE *117210 : CEREBELLAR ATAXIA, AUTOSOMAL DOMINANT PURE #117300 : DEMENTIA, FAMILIAL DANISH; FDD *117340 : CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 2; CDR2 *117350 : CEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS 117360 : CEREBELLAR VERMIS APLASIA *117400 : CEREBELLOPARENCHYMAL DISORDER I; CPD I #117550 : SOTOS SYNDROME 117600 : CEREBRAL SARCOMA 117650 : CEREBROCOSTOMANDIBULAR SYNDROME *117700 : CERULOPLASMIN; CP *117800 : CERUMEN, VARIATION IN 117850 : CERVICAL HYPERTRICHOSIS WITH UNDERLYING KYPHOSCOLIOSIS 117900 : CERVICAL RIB 118000 : CERVICAL VERTEBRAL BRIDGE 118005 : CERVICAL VERTEBRAL DYSPLASIA *118100 : CERVICAL VERTEBRAL FUSION, AUTOSOMAL DOMINANT ^118150 : MOVED TO 107776 *118190 : HEAT-SHOCK 60-KD PROTEIN 1; HSPD1 #118200 : CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B; CMT1B #118210 : CHARCOT-MARIE-TOOTH DISEASE, NEURONAL TYPE, A; CMT2A #118220 : CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A; CMT1A 118230 : CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE #118300 : CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS 118301 : CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM 118330 : CHEILITIS GLANDULARIS 118350 : CHEMODECTOMA, INTRAABDOMINAL, WITH CUTANEOUS ANGIOLIPOMAS #118400 : CHERUBISM 118420 : CHIARI MALFORMATION TYPE I *118423 : CHIMERIN 1; CHN1 *118425 : CHLORIDE CHANNEL 1, SKELETAL MUSCLE; CLCN1 118430 : CHLORPROPAMIDE-ALCOHOL FLUSHING; CPAF *118440 : CHOLECYSTOKININ; CCK *118444 : CHOLECYSTOKININ A RECEPTOR; CCKAR *118445 : CHOLECYSTOKININ B RECEPTOR; CCKBR #118450 : ALAGILLE SYNDROME; AGS *118455 : CYTOCHROME P450, SUBFAMILY VIIA, POLYPEPTIDE 1; CYP7A1 *118457 : CHOLESTEROL CRYSTALLIZATION INHIBITOR; CCI *118470 : CHOLESTERYL ESTER TRANSFER PROTEIN, PLASMA; CETP *118480 : CHOLESTEROL REPRESSIBLE PROTEIN 39B; CHR39B *118485 : CYTOCHROME P450, SUBFAMILY XIA; CYP11A *118490 : CHOLINE ACETYLTRANSFERASE; CHAT *118491 : CHOLINE KINASE; CHK *118493 : CHOLINERGIC RECEPTOR, MUSCARINIC, 2; CHRM2 *118494 : CHOLINERGIC RECEPTOR, MUSCARINIC, 3; CHRM3 *118495 : CHOLINERGIC RECEPTOR, MUSCARINIC, 4; CHRM4 *118496 : CHOLINERGIC RECEPTOR, MUSCARINIC, 5; CHRM5 *118502 : CHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, ALPHA POLYPEPTIDE 2; CHRNA2 *118503 : CHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, ALPHA POLYPEPTIDE 3; CHRNA3 *118504 : CHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, ALPHA POLYPEPTIDE 4; CHRNA4 *118505 : CHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, ALPHA POLYPEPTIDE 5; CHRNA5 *118507 : CHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, BETA POLYPEPTIDE 2; CHRNB2 *118508 : CHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, BETA POLYPEPTIDE 3; CHRNB3 *118509 : CHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, BETA POLYPEPTIDE 4; CHRNB4 *118510 : CHOLINERGIC RECEPTOR, MUSCARINIC, 1; CHRM1 *118511 : CHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, ALPHA POLYPEPTIDE 7; CHRNA7 *118600 : CHONDROCALCINOSIS 2; CCAL2 118610 : CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION *118650 : CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANT 118651 : CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE *118661 : CHONDROITIN SULFATE PROTEOGLYCAN 2; CSPG2 118670 : CHONDRONECTIN *118700 : CHOREA, HEREDITARY BENIGN; BCH 118750 : CHOREOATHETOSIS, FAMILIAL INVERTED *118800 : PAROXYSMAL NONKINESIGENIC DYSKINESIA; PNKD *118820 : CHORIONIC SOMATOMAMMOTROPIN HORMONE 2; CSH2 *118825 : CHOROIDEREMIA-LIKE; CHML *118830 : CHYLOMICRONEMIA, FAMILIAL, DUE TO CIRCULATING INHIBITOR OF LIPOPROTEIN LIPASE *118840 : CHROMATE RESISTANCE; CHR *118850 : CHORIONIC GONADOTROPIN, ALPHA CHAIN; CGA *118860 : CHORIONIC GONADOTROPIN, BETA CHAIN; CGB 118865 : CHOROIDAL OSTEOMA, BILATERAL *118870 : CHROMOSOMAL PROTEIN, NONHISTONE 1; NHCP1 *118880 : CHROMOSOMAL PROTEIN, NONHISTONE 2; NHCP2 *118888 : CHYMOTRYPSIN-LIKE PROTEASE; CTRL *118890 : CHYMOTRYPSINOGEN B1; CTRB1 118900 : CIRRHOSIS, FAMILIAL *118910 : CHROMOGRANIN A; CHGA *118920 : CHROMOGRANIN B; CHGB *118930 : SECRETOGRANIN II; SCG2 *118938 : CHYMASE 1; CMA1 ^118940 : MOVED TO 118938 118943 : CHYMOSIN PSEUDOGENE; CYMP *118945 : CILIARY NEUROTROPHIC FACTOR; CNTF *118946 : CILIARY NEUROTROPHIC FACTOR RECEPTOR; CNTFR *118950 : CITRATE SYNTHASE, MITOCHONDRIAL; CS ^118953 : MOVED TO 192020 *118955 : CLATHRIN, HEAVY POLYPEPTIDE; CLTC *118960 : CLATHRIN, LIGHT POLYPEPTIDE A; CLTA *118970 : CLATHRIN, LIGHT POLYPEPTIDE B; CLTB 118980 : CLAVICLE, PSEUDARTHROSIS OF, CONGENITAL *118990 : SPERM-SPECIFIC ANTIGEN 2; SSFA2 *119000 : CLEFT CHIN *119100 : CLEFT HAND AND ABSENT TIBIA *119300 : VAN DER WOUDE SYNDROME; VWS *119500 : POPLITEAL PTERYGIUM SYNDROME; PPS *119530 : OROFACIAL CLEFT 1; OFC1 *119540 : CLEFT PALATE, ISOLATED; CPI *119550 : CLEFT PALATE-LATERAL SYNECHIA SYNDROME 119570 : CLEFT SOFT PALATE 119580 : BLEPHAROCHEILODONTIC SYNDROME #119600 : CLEIDOCRANIAL DYSPLASIA; CCD 119650 : CLEIDORHIZOMELIC SYNDROME 119800 : CLUBFOOT *119900 : CLUBBING OF DIGITS 119915 : CLUSTER HEADACHE, FAMILIAL 120000 : COARCTATION OF AORTA 120040 : COCHLEOSACCULAR DEGENERATION OF THE INNER EAR WITH PROGRESSIVE CATARACTS *120050 : COXSACKIE B3 VIRUS SUSCEPTIBILITY; CXB3S *120070 : COLLAGEN, TYPE IV, ALPHA-3; COL4A3 #120080 : COLCHICINE RESISTANCE *120090 : COLLAGEN, TYPE IV, ALPHA-2; COL4A2 #120100 : FAMILIAL COLD AUTOINFLAMMATORY SYNDROME; FCAS *120105 : COLIPASE, PANCREATIC; CLPS *120110 : COLLAGEN, TYPE X, ALPHA-1; COL10A1 *120120 : COLLAGEN, TYPE VII, ALPHA-1; COL7A1 *120130 : COLLAGEN, TYPE IV, ALPHA-1; COL4A1 *120131 : COLLAGEN, TYPE IV, ALPHA-4; COL4A4 *120140 : COLLAGEN, TYPE II, ALPHA-1; COL2A1 *120150 : COLLAGEN, TYPE I, ALPHA-1; COL1A1 *120160 : COLLAGEN, TYPE I, ALPHA-2; COL1A2 *120165 : COLLAGEN, TYPE XIX, ALPHA-1; COL19A1 *120170 : COLLAGEN, FETAL MEMBRANE, B POLYPEPTIDE *120180 : COLLAGEN, TYPE III, ALPHA-1; COL3A1 *120190 : COLLAGEN, TYPE V, ALPHA-2; COL5A2 *120200 : COLOBOMA OF IRIS, CHOROID AND RETINA; COI *120210 : COLLAGEN, TYPE IX, ALPHA-1; COL9A1 *120215 : COLLAGEN, TYPE V, ALPHA-1; COL5A1 *120216 : COLLAGEN, TYPE V, ALPHA-3; COL5A3 *120220 : COLLAGEN, TYPE VI, ALPHA-1; COL6A1 *120240 : COLLAGEN, TYPE VI, ALPHA-2; COL6A2 *120250 : COLLAGEN, TYPE VI, ALPHA-3; COL6A3 *120251 : COLLAGEN, TYPE VIII, ALPHA-1; COL8A1 *120252 : COLLAGEN, TYPE VIII, ALPHA-2; COL8A2 *120260 : COLLAGEN, TYPE IX, ALPHA-2; COL9A2 *120270 : COLLAGEN, TYPE IX, ALPHA-3; COL9A3 *120280 : COLLAGEN, TYPE XI, ALPHA-1; COL11A1 *120290 : COLLAGEN, TYPE XI, ALPHA-2; COL11A2 *120300 : COLOBOMA OF MACULA ^120310 : MOVED TO 120140 *120320 : COLLAGEN, TYPE XII, ALPHA-1; COL12A1 *120321 : COLLAGEN, TYPE XII, ALPHA 1-LIKE *120324 : COLLAGEN, TYPE XIV, ALPHA-1; COL14A1 *120325 : COLLAGEN, TYPE XV, ALPHA-1; COL15A1 *120326 : COLLAGEN, TYPE XVI, ALPHA-1; COL16A1 ^120327 : MOVED TO 113811 *120328 : COLLAGEN, TYPE XVIII, ALPHA-1; COL18A1 #120330 : RENAL-COLOBOMA SYNDROME *120340 : COLLAGEN, TYPE I, ALPHA, RECEPTOR; COL1AR *120350 : COLLAGEN, TYPE XIII, ALPHA-1; COL13A1 *120353 : MATRIX METALLOPROTEINASE 1; MMP1 *120355 : MATRIX METALLOPROTEINASE 8; MMP8 *120360 : MATRIX METALLOPROTEINASE 2; MMP2 *120361 : MATRIX METALLOPROTEINASE 9; MMP9 120400 : COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY *120420 : COLONY-STIMULATING FACTOR 1; CSF1 120430 : COLOBOMA OF OPTIC NERVE 120433 : COLOBOMA, UVEAL, WITH CLEFT LIP AND PALATE AND MENTAL RETARDATION *120435 : COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 1 *120436 : COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 2 120440 : COLONIC VARICES WITHOUT PORTAL HYPERTENSION *120450 : COMEDONES, FAMILIAL DYSKERATOTIC ^120460 : MOVED TO 191170 *120470 : DELETED IN COLORECTAL CARCINOMA; DCC 120500 : COMMISSURAL LIP PITS *120502 : BRANCHIOOTIC SYNDROME 2 *120520 : MEMBRANE METALLOENDOPEPTIDASE; MME *120550 : COMPLEMENT COMPONENT 1, q SUBCOMPONENT, ALPHA POLYPEPTIDE; C1QA *120560 : COMPLEMENT COMPONENT C1q, FIBROBLAST TYPE *120570 : COMPLEMENT COMPONENT 1, q SUBCOMPONENT, BETA POLYPEPTIDE; C1QB *120575 : COMPLEMENT COMPONENT 1, q SUBCOMPONENT, GAMMA POLYPEPTIDE; C1QG *120577 : COMPLEMENT COMPONENT 1, q SUBCOMPONENT, RECEPTOR 1; C1QR1 *120580 : COMPLEMENT COMPONENT 1, s SUBCOMPONENT; C1S *120620 : COMPLEMENT COMPONENT RECEPTOR 1; CR1 *120650 : COMPLEMENT COMPONENT RECEPTOR 2; CR2 *120700 : COMPLEMENT COMPONENT 3; C3 #120790 : COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF *120810 : COMPLEMENT COMPONENT 4A; C4A *120820 : COMPLEMENT COMPONENT 4B; C4B *120830 : COMPLEMENT COMPONENT 4-BINDING PROTEIN, ALPHA; C4BPA *120831 : COMPLEMENT COMPONENT 4-BINDING PROTEIN, BETA CHAIN; C4BPB ^120832 : MOVED TO 120830 *120900 : COMPLEMENT COMPONENT 5 DEFICIENCY *120920 : MEMBRANE COFACTOR PROTEIN; MCP *120930 : COMPLEMENT COMPONENT 8, GAMMA SUBUNIT; C8G *120940 : COMPLEMENT COMPONENT 9; C9 *120950 : COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I *120960 : COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II #120970 : CONE-ROD DYSTROPHY 2; CORD2 *120980 : INTEGRIN, ALPHA-M; ITGAM ^121000 : REMOVED FROM DATABASE *121009 : CONNECTIVE TISSUE GROWTH FACTOR; CTGF *121010 : PRO-PLATELET BASIC PROTEIN; PPBP *121011 : GAP JUNCTION PROTEIN, BETA-2; GJB2 *121012 : GAP JUNCTION PROTEIN, ALPHA-4; GJA4 *121013 : GAP JUNCTION PROTEIN, ALPHA-5; GJA5 *121014 : GAP JUNCTION PROTEIN, ALPHA-1; GJA1 *121015 : GAP JUNCTION PROTEIN, ALPHA-3; GJA3 121020 : CONTINUOUS MUSCLE FIBER ACTIVITY, HEREDITARY *121050 : CONTRACTURAL ARACHNODACTYLY, CONGENITAL 121070 : CONTRACTURES OF FINGERS AND JAW #121200 : EPILEPSY, BENIGN NEONATAL, 1; EBN1 #121201 : EPILEPSY, BENIGN NEONATAL, 2; EBN2 #121210 : FEBRILE SEIZURES ^121250 : MOVED TO 300088 121270 : COPPER DEFICIENCY, FAMILIAL BENIGN *121300 : COPROPORPHYRIA 121350 : CORACOCLAVICULAR JOINT, ANOMALOUS *121360 : CORE-BINDING FACTOR, BETA SUBUNIT; CBFB *121390 : CORNEA GUTTATA WITH ANTERIOR POLAR CATARACTS *121400 : CORNEA PLANA 1; CNA1 121450 : CORNEAL DEGENERATION, RIBBONLIKE, WITH DEAFNESS *121700 : CORNEAL ENDOTHELIAL DYSTROPHY 1; CHED1 *121800 : CORNEAL DYSTROPHY, CRYSTALLINE, OF SCHNYDER 121820 : CORNEAL DYSTROPHY, EPITHELIAL BASEMENT MEMBRANE *121850 : CORNEAL DYSTROPHY, FRANCOIS-NEETENS SPECKLED OR FLECKED #121900 : CORNEAL DYSTROPHY, GRANULAR TYPE #122000 : CORNEAL DYSTROPHY, HEREDITARY POLYMORPHOUS POSTERIOR #122100 : CORNEAL DYSTROPHY, JUVENILE EPITHELIAL, OF MEESMANN #122200 : CORNEAL DYSTROPHY, LATTICE TYPE I; CDL1 *122400 : CORNEAL EROSIONS, RECURRING HEREDITARY 122430 : CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS, UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION 122440 : CORNEODERMATOOSSEOUS SYNDROME *122450 : CORNEAL HYPESTHESIA, FAMILIAL 122455 : CORONARY ARTERY DISSECTION, SPONTANEOUS *122460 : CORONAVIRUS 229E SUSCEPTIBILITY; CVS 122470 : CORNELIA DE LANGE SYNDROME 1; CDL1 ^122480 : MOVED TO 166740 *122500 : CORTICOSTEROID-BINDING GLOBULIN; CBG 122550 : CORTICOSTERONE SIDE-CHAIN ISOMERASE; CSCI *122559 : CORTICOTROPIN RELEASING HORMONE-BINDING PROTEIN; CRHBP *122560 : CORTICOTROPIN-RELEASING HORMONE; CRH *122561 : CORTICOTROPIN-RELEASING HORMONE RECEPTOR 1; CRHR1 122580 : COSTOCORACOID LIGAMENT, CONGENITALLY SHORT *122600 : COSTOVERTEBRAL SEGMENTATION ANOMALIES #122700 : COUMARIN RESISTANCE *122720 : CYTOCHROME P450, SUBFAMILY IIA, POLYPEPTIDE 6; CYP2A6 *122750 : COXA VARA 122780 : COXOAURICULAR SYNDROME 122850 : CRANIOACROFACIAL SYNDROME 122860 : CRANIODIAPHYSEAL DYSPLASIA, DOMINANT #122880 : CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS 122900 : CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA 122920 : CRANIOFRONTAL DYSPLASIA #123000 : CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CMDD 123050 : CRANIORHINY *123100 : CRANIOSYNOSTOSIS, TYPE 1; CRS1 *123101 : MUSCLE SEGMENT HOMEO BOX, DROSOPHILA, HOMOLOG OF, 2; MSX2 #123150 : JACKSON-WEISS SYNDROME; JWS 123155 : CRANIOSYNOSTOSIS, SAGITTAL, WITH DANDY-WALKER MALFORMATION AND HYDROCEPHALUS *123260 : C-REACTIVE PROTEIN, PENTRAXIN-RELATED; CRP 123270 : CREATINE KINASE, BRAIN TYPE, ECTOPIC EXPRESSION OF; CKBE *123280 : CREATINE KINASE, BRAIN TYPE; CKB *123290 : CREATINE KINASE, MITOCHONDRIAL; CKMT *123295 : CREATINE KINASE, SARCOMERIC MITOCHONDRIAL; CKMTS *123310 : CREATINE KINASE, MUSCLE TYPE; CKM #123320 : CREATINE PHOSPHOKINASE, ELEVATED SERUM #123400 : CREUTZFELDT-JAKOB DISEASE; CJD #123450 : CRI-DU-CHAT SYNDROME #123500 : CROUZON SYNDROME 123540 : CRYOFIBRINOGENEMIA, FAMILIAL PRIMARY *123550 : CRYOGLOBULINEMIA, FAMILIAL MIXED *123555 : CRYPTDIN-RELATED SEQUENCE 1C; CRS1C 123557 : CRYPTOTIA, FAMILIAL 123560 : CRYPTOMICROTIA-BRACHYDACTYLY SYNDROME *123570 : CRYPTOPHTHALMOS, UNILATERAL OR BILATERAL, ISOLATED *123580 : CRYSTALLIN, ALPHA-A; CRYAA *123590 : CRYSTALLIN, ALPHA-B; CRYAB *123610 : CRYSTALLIN, BETA-A1; CRYBA1 *123620 : CRYSTALLIN, BETA-B2; CRYBB2 *123630 : CRYSTALLIN, BETA-B3; CRYBB3 *123631 : CRYSTALLIN, BETA-A4; CRYBA4 *123660 : CRYSTALLIN, GAMMA-A; CRYGA *123670 : CRYSTALLIN, GAMMA-B; CRYGB *123680 : CRYSTALLIN, GAMMA-C; CRYGC *123690 : CRYSTALLIN, GAMMA-D; CRYGD *123691 : CRYSTALLIN, ZETA; CRYZ *123695 : PHOSPHATE CYTIDYLYLTRANSFERASE 1, CHOLINE, ALPHA ISOFORM; PCYT1A #123700 : CUTIS LAXA ^123710 : MOVED TO 123660 ^123720 : MOVED TO 123660 *123730 : CRYSTALLIN, GAMMA-S; CRYGS *123740 : CRYSTALLIN, MU; CRYM #123790 : CUTIS GYRATA SYNDROME OF BEARE AND STEVENSON *123803 : ACTIVATING TRANSCRIPTION FACTOR 1; ATF1 *123805 : PHOSPHODIESTERASE 3A, cGMP-INHIBITED; PDE3A *123810 : cAMP RESPONSE ELEMENT-BINDING PROTEIN 1; CREB1 *123811 : ACTIVATING TRANSCRIPTION FACTOR 2; ATF2 *123812 : cAMP RESPONSE ELEMENT MODULATOR; CREM *123825 : CYCLIC NUCLEOTIDE-GATED CHANNEL, ALPHA-1; CNGA1 *123828 : CYCLIN-DEPENDENT KINASE 3; CDK3 *123829 : CYCLIN-DEPENDENT KINASE 4; CDK4 *123830 : CYCLIC NUCLEOTIDE PHOSPHODIESTERASE; CNP *123831 : CYCLIN-DEPENDENT KINASE 5; CDK5 *123832 : CYCLIN-DEPENDENT KINASE INHIBITOR 3; CDKN3 *123833 : CYCLIN D2; CCND2 *123834 : CYCLIN D3; CCND3 *123835 : CYCLIN A2; CCNA2 *123836 : CYCLIN B1; CCNB1 *123837 : CYCLIN E1; CCNE1 *123838 : CYCLIN C; CCNC ^123839 : MOVED TO 600262 *123840 : PEPTIDYL-PROLYL ISOMERASE A; PPIA *123841 : PEPTIDYL-PROLYL ISOMERASE B; PPIB *123842 : PEPTIDYL-PROLYL ISOMERASE C; PPIC ^123850 : MOVED TO 132700 123853 : CYPRUS FACIAL NEUROMUSCULOSKELETAL SYNDROME *123855 : CYSTATIN 1; CST1 *123856 : CYSTATIN 2; CST2 *123857 : CYSTATIN 4; CST4 *123858 : CYSTATIN 5; CST5 *123859 : CYSTEINYL-tRNA SYNTHETASE; CARS *123860 : CYTIDINE 5-PRIME TRIPHOSPHATE SYNTHETASE; CTPS *123864 : CYTOCHROME c OXIDASE, SUBUNIT IV, ISOFORM 1; COX4I1 *123866 : CYTOCHROME c OXIDASE, SUBUNIT Vb; COX5B *123870 : CYTOCHROME c OXIDASE, SUBUNIT VIII; COX8 *123875 : CYSTEINE-RICH INTESTINAL PROTEIN 1; CRIP1 *123876 : CYSTEINE- AND GLYCINE-RICH PROTEIN 1; CSRP1 123880 : CYSTIC ANGIOMATOSIS OF BONE, DIFFUSE *123885 : S100 CALCIUM-BINDING PROTEIN A8; S100A8 *123886 : S100 CALCIUM-BINDING PROTEIN A9; S100A9 *123889 : INTERLEUKIN 10 RECEPTOR, BETA; IL10RB *123890 : CYTOTOXIC T LYMPHOCYTE-ASSOCIATED 4; CTLA4 *123900 : VILLIN 2; VIL2 *123910 : GRANZYME B; GZMB *123920 : CYTIDINE DEAMINASE; CDA *123930 : CYTOCHROME P450, SUBFAMILY IIB; CYP2B *123940 : KERATIN 4; KRT4 ^123950 : MOVED TO 250790 *123960 : CYTOCHROME P450, SUBFAMILY IIA; CYP2A *123970 : CYTOCHROME C *123980 : CYTOCHROME C1; CYC1 *123995 : CYTOCHROME c OXIDASE, SUBUNIT VIIa, POLYPEPTIDE 1; COX7A1 *123996 : CYTOCHROME c OXIDASE, SUBUNIT VIIa, POLYPEPTIDE 2; COX7A2 *123997 : CYTOCHROME c OXIDASE, SUBUNIT VIIa, POLYPEPTIDE 3; COX7A3 124000 : CYTOCHROME-RELATED DISEASE OF MUSCLE AND NERVOUS SYSTEM *124010 : CYTOCHROME P450, SUBFAMILY IIIA, POLYPEPTIDE 4; CYP3A4 *124015 : CYTOCHROME P-450 REDUCTASE; POR *124020 : CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19 *124030 : CYTOCHROME P450, SUBFAMILY IID; CYP2D *124040 : CYTOCHROME P450, SUBFAMILY IIE; CYP2E *124050 : D-AMINO ACID OXIDASE; DAO *124060 : CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 2; CYP1A2 *124070 : CYTOCHROME P450, SUBFAMILY IIF, POLYPEPTIDE 1; CYP2F1 *124075 : CYTOCHROME P450, SUBFAMILY IVB, MEMBER 1; CYP4B1 *124080 : CYTOCHROME P450, SUBFAMILY XIB, POLYPEPTIDE 2; CYP11B2 *124089 : CYTOCHROME c OXIDASE, SUBUNIT VIb; COX6B *124090 : CYTOCHROME c OXIDASE, SUBUNIT VIc; COX6C *124092 : INTERLEUKIN 10; IL10 *124095 : CYTOPLASMIC TYROSINE KINASE; CSK *124097 : D SITE OF ALBUMIN PROMOTER-BINDING PROTEIN; DBP 124100 : DANUBIAN ENDEMIC FAMILIAL NEPHROPATHY #124200 : DARIER-WHITE DISEASE; DAR 124300 : DARWINIAN POINT OF PINNA 124400 : DARWINIAN TUBERCLE OF PINNA *124450 : D-ASPARTATE OXIDASE *124480 : DEAFNESS AND ONYCHODYSTROPHY, DOMINANT FORM 124490 : DEAFNESS, CONDUCTIVE STAPEDIAL, WITH EAR MALFORMATION AND FACIAL PALSY #124500 : DEAFNESS, CONGENITAL, WITH KERATOPACHYDERMIA AND CONSTRICTIONS OF FINGERS AND TOES ^124580 : REMOVED FROM DATABASE *124700 : DEAFNESS, MID-TONE NEURAL *124800 : DEAFNESS, PROGRESSIVE HIGH-TONE NEURAL #124900 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 1; DFNA1 124910 : DEAFNESS: LOW-FREQUENCY HEARING LOSS, MIXED CONDUCTIVE-SENSORINEURAL TYPE 124950 : DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE 125000 : DEAFNESS, UNILATERAL 125050 : DEAFNESS WITH ANHIDROTIC ECTODERMAL DYSPLASIA 125100 : DEAFNESS WITH EAR PITS *125220 : DEFENSIN, ALPHA, 1; DEFA1 125230 : DEAFNESS-CRANIOFACIAL SYNDROME *125240 : DECAY-ACCELERATING FACTOR FOR COMPLEMENT; DAF 125250 : DEAFNESS--OPTIC ATROPHY SYNDROME *125255 : DECORIN; DCN *125260 : DEFECTIVE INTERFERING PARTICLE INDUCTION, CONTROL OF *125263 : SULFOTRANSFERASE FAMILY 2A, DEHYDROEPIANDROSTERONE-PREFERRING, MEMBER 1; SULT2A1 *125264 : DEK ONCOGENE; DEK *125265 : DELETED IN POLYPOSIS 1 *125270 : DELTA-AMINOLEVULINATE DEHYDRATASE; ALAD 125280 : DENS EVAGINATUS *125290 : DELTA-AMINOLEVULINATE SYNTHASE; ALAS1 125300 : DENS IN DENTE AND PALATAL INVAGINATIONS *125305 : ERYTHROCYTE MEMBRANE PROTEIN BAND 4.9; EPB49 #125310 : CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CADASIL 125320 : DEMENTIA/PARKINSONISM WITH NON-ALZHEIMER AMYLOID PLAQUES 125350 : DENTAL NONERUPTION *125370 : DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY; DRPLA *125400 : DENTIN DYSPLASIA, TYPE I *125420 : DENTIN DYSPLASIA, TYPE II *125440 : DENTIN DYSPLASIA WITH SCLEROTIC BONES *125450 : DEOXYCYTIDINE KINASE; DCK 125460 : DEOXYRIBOSE-5-PHOSPHATE ALDOLASE DEFICIENCY *125480 : MAJOR AFFECTIVE DISORDER 1; MAFD1 *125485 : DENTIN SIALOPHOSPHOPROTEIN; DSPP #125490 : DENTINOGENESIS IMPERFECTA 1; DGI1 125500 : DENTINOGENESIS IMPERFECTA, SHIELDS TYPE III *125505 : DEOXYRIBONUCLEASE I; DNASE1 ^125510 : REMOVED FROM DATABASE *125520 : DEPRESSOR ANGULI ORIS MUSCLE, HYPOPLASIA OF 125530 : DERMAL RIDGES, NELSON SYNDROME *125540 : DERMAL RIDGES, PATTERNLESS *125550 : DERMAL RIDGES-OFF-THE-END 125570 : DERMATOGLYPHICS--ARCH ON ANY DIGIT 125580 : DERMATOGLYPHICS--FINGER RIDGE COUNT 125590 : DERMATOGLYPHICS--FINGERPRINT PATTERN 125595 : DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR *125597 : DERMATOPONTIN; DPT 125600 : DERMATOSIS PAPULOSA NIGRA 125630 : DERMODISTORTIVE URTICARIA; DDU 125635 : DERMOGRAPHISM, FAMILIAL 125640 : DERMOODONTODYSPLASIA *125643 : DESMOCOLLIN 1; DSC1 *125645 : DESMOCOLLIN 2; DSC2 *125647 : DESMOPLAKIN; DSP *125650 : DESMOSTEROL-TO-CHOLESTEROL ENZYME; DCE *125660 : DESMIN; DES *125670 : DESMOGLEIN 1; DSG1 *125671 : DESMOGLEIN 2; DSG2 #125700 : DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE #125800 : DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL DOMINANT #125850 : MATURITY-ONSET DIABETES OF THE YOUNG, TYPE I; MODY1 #125851 : MATURITY-ONSET DIABETES OF THE YOUNG, TYPE II; MODY2 *125852 : DIABETES MELLITUS, INSULIN-DEPENDENT, 2 #125853 : DIABETES MELLITUS, NONINSULIN-DEPENDENT; NIDDM *125855 : DIACYLGLYCEROL KINASE, ALPHA, 80-KD; DGKA *125860 : NAD(P)H DEHYDROGENASE, QUINONE 1; NQO1 *125870 : DIAPHORASE 2; DIA2 *125880 : DIAPHORASE 3; DIA3 125890 : DIARRHEA, GLUCOSE-STIMULATED SECRETORY, WITH COMMON VARIABLE IMMUNODEFICIENCY 125900 : DIASTEMA, DENTAL MEDIAL *125950 : DIAZEPAM BINDING INHIBITOR; DBI *126050 : DIGITOTALAR DYSMORPHISM *126060 : DIHYDROFOLATE REDUCTASE; DHFR ^126061 : MOVED TO 126060 *126063 : DIHYDROLIPOAMIDE S-SUCCINYLTRANSFERASE; DLST *126064 : DIHYDROOROTATE DEHYDROGENASE; DHODH *126065 : CYTOCHROME P450, SUBFAMILY XXIV; CYP24 *126070 : DILUTION, PIGMENTARY *126090 : PTERIN-4-ALPHA-CARBINOLAMINE DEHYDRATASE; PCBD 126100 : DIMPLES, FACIAL *126110 : ARYL HYDROCARBON RECEPTOR NUCLEAR TRANSLOCATOR; ARNT ^126140 : MOVED TO 102720 *126141 : DIPEPTIDYL PEPTIDASE IV-RELATED PROTEIN; DPPX *126150 : DIPHTHERIA TOXIN RECEPTOR; DTR 126180 : DISCRIMINATION, TWO-POINT, REDUCTION IN 126190 : DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS #126200 : MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO; MS 126250 : DISTAL OSTEOSCLEROSIS *126255 : DISTAL-LESS HOMEO BOX 2; DLX2 *126300 : DISTICHIASIS 126320 : DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL VASCULATURE *126330 : DNA, CYTOPLASMIC-MEMBRANE; DNCM *126335 : GROWTH ARREST- AND DNA DAMAGE-INDUCIBLE GENE GADD45, ALPHA; GADD45A *126337 : DNA DAMAGE-INDUCIBLE TRANSCRIPT 3; DDIT3 *126340 : EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 2; ERCC2 *126350 : DEOXYRIBONUCLEASE II, LYSOSOMAL; DNASE2 126370 : DNA, SATELLITE, III; HS3; D1Z1 *126375 : DNA METHYLTRANSFERASE 1; DNMT1 *126380 : EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 1; ERCC1 126390 : DNA, LOW-REPETITIVE SEQUENCES OF *126391 : LIGASE I, DNA, ATP-DEPENDENT; LIG1 126410 : DNA, SATELLITE, ALPHA TYPE *126420 : TOPOISOMERASE, DNA, I; TOP1 *126430 : TOPOISOMERASE, DNA, II, ALPHA; TOP2A *126431 : TOPOISOMERASE, DNA, II, BETA; TOP2B ^126440 : REMOVED FROM DATABASE ^126448 : MOVED TO 126453 *126449 : DOPAMINE RECEPTOR D1; DRD1 *126450 : DOPAMINE RECEPTOR D2; DRD2 *126451 : DOPAMINE RECEPTOR D3; DRD3 *126452 : DOPAMINE RECEPTOR D4; DRD4 *126453 : DOPAMINE RECEPTOR D5; DRD5 *126455 : SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, DOPAMINE), MEMBER 3; SLC6A3 126500 : DOUBLE NAIL FOR FIFTH TOE *126550 : DOUGHNUT LESIONS OF SKULL, FAMILIAL #126600 : DOYNE HONEYCOMB RETINAL DYSTROPHY; DHRD *126650 : SOLUTE CARRIER FAMILY 26, MEMBER 3; SLC26A3 *126660 : DREBRIN E; DBN1 126700 : DRUSEN OF BRUCH MEMBRANE *126800 : DUANE RETRACTION SYNDROME 1; DURS1 ^126830 : MOVED TO 169100 126840 : DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION *126850 : DUODENAL ULCER, HYPERPEPSINOGENEMIC I *126900 : DUPUYTREN CONTRACTURE 126950 : DWARFISM WITH TALL VERTEBRAE *127000 : KENNY-CAFFEY SYNDROME, TYPE 2 127100 : DWARFISM, LEVI TYPE 127200 : DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES #127300 : LERI-WEILL DYSCHONDROSTEOSIS; LWD 127350 : DYSCHONDROSTEOSIS AND NEPHRITIS *127400 : DYSCHROMATOSIS SYMMETRICA HEREDITARIA; DSH 127500 : DYSCHROMATOSIS UNIVERSALIS HEREDITARIA #127550 : DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT *127600 : DYSKERATOSIS, HEREDITARY BENIGN INTRAEPITHELIAL *127700 : DYSLEXIA, SPECIFIC, 1; DYX1 127750 : DEMENTIA, LEWY BODY 127800 : DYSPLASIA EPIPHYSEALIS HEMIMELICA 127820 : DYSPLASIA EPIPHYSEALIS HEMIMELICA WITH CHONDROMAS AND OSTEOCHONDROMAS *128000 : DYSTELEPHALANGY #128100 : TORSION DYSTONIA 1, AUTOSOMAL DOMINANT; DYT1 *128101 : DYSTONIA MUSCULORUM DEFORMANS 4; DYT4 *128200 : PAROXYSMAL KINESIGENIC CHOREOATHETOSIS; PKC #128230 : DYSTONIA, PROGRESSIVE, WITH DIURNAL VARIATION *128235 : DYSTONIA 12; DYT12 *128239 : DYSTROPHIN-ASSOCIATED GLYCOPROTEIN 1; DAG1 *128240 : UTROPHIN; UTRN *128260 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE E; SNRPE 128290 : EAR ANTITRAGUS, TAG AT BASE OF 128300 : EAR EXOSTOSES 128400 : EAR FLARE 128500 : EAR FOLDING *128600 : EAR MALFORMATION *128700 : EAR PITS 128710 : EAR PITS, POSTERIOR HELICAL 128800 : EAR WITHOUT HELIX 128900 : EARLOBE ATTACHMENT: ATTACHED VS UNATTACHED 128950 : EARLOBE CREASE *128980 : EARLOBES, THICKENED, WITH CONDUCTIVE DEAFNESS FROM INCUDOSTAPEDIAL ABNORMALITIES *128990 : EARLY GROWTH RESPONSE 1; EGR1 *128992 : EARLY GROWTH RESPONSE 4; EGR4 129000 : EARRING HOLES, NATURAL *129010 : EARLY GROWTH RESPONSE 2; EGR2 129100 : EARS, ABILITY TO MOVE *129150 : ECHO 11 SENSITIVITY; E11S *129190 : NUCLEOTIDASE, ECTO-5-PRIME; NT5E *129200 : ECTODERMAL DYSPLASIA, ABSENT DERMATOGLYPHIC PATTERN, CHANGES IN NAILS, AND SIMIAN CREASE *129400 : ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP AND CLEFT PALATE #129490 : ECTODERMAL DYSPLASIA 3, ANHIDROTIC; ED3 #129500 : ECTODERMAL DYSPLASIA 2, HIDROTIC; ED2 129510 : ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE 129540 : ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE AND PREAXIAL POLYDACTYLY OF FEET 129550 : ECTODERMAL DYSPLASIA WITH ADRENAL CYST *129600 : ECTOPIA LENTIS, ISOLATED #129750 : ECTOPIA PUPILLAE 129810 : ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE 129830 : ECTRODACTYLY-CLEFT PALATE SYNDROME 129840 : EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL #129850 : EDINBURGH MALFORMATION SYNDROME *129900 : ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1; EEC1 129905 : EGASYN #130000 : EHLERS-DANLOS SYNDROME, TYPE I; EDS1 #130010 : EHLERS-DANLOS SYNDROME, TYPE II; EDS2 #130020 : EHLERS-DANLOS SYNDROME, TYPE III #130050 : EHLERS-DANLOS SYNDROME, TYPE IV, AUTOSOMAL DOMINANT; EDS4 #130060 : EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT #130070 : EHLERS-DANLOS SYNDROME, PROGEROID FORM *130080 : EHLERS-DANLOS SYNDROME, TYPE VIII 130090 : EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED 130100 : ELASTOSIS PERFORANS SERPIGINOSA; EPS *130120 : ELASTASE 1; ELA1 *130130 : ELASTASE 2; ELA2 *130135 : PROTEASE INHIBITOR 2, MONOCYTE/NEUTROPHIL DERIVED; ELANH2 *130160 : ELASTIN; ELN *130180 : ELECTROENCEPHALOGRAM, LOW-VOLTAGE #130190 : ELECTROENCEPHALOGRAPHIC PATTERNS; EEG 130200 : ELECTROENCEPHALOGRAPHIC PECULIARITY: 14 AND 6 PER SEC. POSITIVE SPIKE PHENOMENON 130300 : ELECTROENCEPHALOGRAPHIC PECULIARITY: FRONTO-PRECENTRAL BETA WAVE GROUPS 130400 : ELECTROENCEPHALOGRAPHIC PECULIARITY: OCCIPITAL SLOW BETA WAVES *130410 : ELECTRON TRANSFER FLAVOPROTEIN, BETA POLYPEPTIDE; ETFB *130500 : ERYTHROCYTE MEMBRANE PROTEIN BAND 4.1; EPB41 *130590 : EUKARYOTIC TRANSLATION ELONGATION FACTOR 1, ALPHA-1; EEF1A1 *130591 : EUKARYOTIC TRANSLATION ELONGATION FACTOR 1, BETA-1; EEF1B1 *130592 : EUKARYOTIC TRANSLATION ELONGATION FACTOR 1, DELTA; EEF1D *130593 : EUKARYOTIC TRANSLATION ELONGATION FACTOR 1, GAMMA; EEF1G #130600 : ELLIPTOCYTOSIS, RHESUS-UNLINKED TYPE *130610 : EUKARYOTIC TRANSLATION ELONGATION FACTOR 2; EEF2 *130620 : RIBOSOMAL PROTEIN S14; RPS14 #130650 : BECKWITH-WIEDEMANN SYNDROME; BWS *130660 : EMILIN 130700 : EMPHYSEMA, HEREDITARY PULMONARY 130710 : EMPHYSEMA, CONGENITAL LOBAR; CLE 130720 : EMPTY SELLA TURCICA, PRIMARY, WITH GENERALIZED DYSPLASIA 130900 : ENAMEL HYPOPLASIA, HEREDITARY LOCALIZED 130950 : ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD *131100 : MULTIPLE ENDOCRINE NEOPLASIA, TYPE I; MEN1 *131150 : ENDOGENOUS RETROVIRAL SEQUENCE 1; ERV1 *131170 : ENDOGENOUS RETROVIRAL SEQUENCE 3; ERV3 *131180 : ENDOGENOUS RETROVIRAL POL-LIKE SEQUENCE-2; ERPL2 *131190 : ENDOGENOUS RETROVIRAL POL-LIKE SEQUENCE-1; ERPL1 *131195 : ENDOGLIN; ENG 131200 : ENDOMETRIOSIS *131210 : SELECTIN E; SELE *131220 : FIBROBLAST GROWTH FACTOR 1; FGF1 *131222 : ENDOTHELIAL CELL GROWTH FACTOR, PLATELET-DERIVED; ECGF1 *131230 : ANNEXIN A5; ANXA5 *131235 : ENDOPLASMIC RETICULUM KDEL RECEPTOR *131240 : ENDOTHELIN 1; EDN1 *131241 : ENDOTHELIN 2; EDN2 *131242 : ENDOTHELIN 3; EDN3 *131243 : ENDOTHELIN RECEPTOR, TYPE A; EDNRA *131244 : ENDOTHELIN RECEPTOR, TYPE B; EDNRB *131290 : ENGRAILED 1; EN1 #131300 : CAMURATI-ENGELMANN DISEASE *131310 : ENGRAILED 2; EN2 *131320 : GATA-BINDING PROTEIN 3; GATA3 *131330 : PROENKEPHALIN; PENK *131340 : PRODYNORPHIN; PDYN *131360 : ENOLASE 2; ENO2 *131370 : ENOLASE 3; ENO3 131375 : ENOLASE, SPERM SPECIFIC; ENO4 *131390 : NIDOGEN; NID *131398 : RIBONUCLEASE A FAMILY, 3; RNASE3 *131399 : EOSINOPHIL PEROXIDASE; EPX *131400 : EOSINOPHILIA, FAMILIAL *131410 : RIBONUCLEASE A FAMILY, 2; RNASE2 131430 : EOSINOPHILOPENIA 131440 : EOSINOPHILS, MALIGNANT PROLIFERATION OF 131445 : EPENDYMOMA, FAMILIAL 131450 : EPIBLEPHARON OF LOWER LID 131460 : EPIBLEPHARON OF UPPER LID *131500 : EPICANTHUS *131530 : EPIDERMAL GROWTH FACTOR; EGF *131550 : EPIDERMAL GROWTH FACTOR RECEPTOR; EGFR *131560 : FLOTILLIN 2; FLOT2 131600 : EPIDERMOID CYSTS #131705 : TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN; TBDN #131750 : EPIDERMOLYSIS BULLOSA DYSTROPHICA, PASINI TYPE #131760 : EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE #131800 : EPIDERMOLYSIS BULLOSA OF HANDS AND FEET #131850 : EPIDERMOLYSIS BULLOSA, PRETIBIAL 131880 : EPIDERMOLYSIS BULLOSA WITH DEFICIENCY OF GALACTOSYLHYDROXYLYSYL GLUCOSYLTRANSFERASE #131900 : EPIDERMOLYSIS BULLOSA SIMPLEX, KOEBNER TYPE; EBS2 *131950 : EPIDERMOLYSIS BULLOSA SIMPLEX, OGNA TYPE #131960 : EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION; EBS-MP #132000 : EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN AND DEFORMITY OF NAILS 132090 : EPILEPSY, BENIGN OCCIPITAL; BOE 132100 : EPILEPSY, PHOTOGENIC 132300 : EPILEPSY, READING *132350 : EPIMORPHIN; EPIM #132400 : EPIPHYSEAL DYSPLASIA, MULTIPLE, 1; EDM1 #132450 : EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS 132500 : EPISTAXIS, HEREDITARY #132600 : PILOMATRIXOMA #132700 : CYLINDROMATOSIS, FAMILIAL; CYLD *132800 : MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA; MSSE *132810 : EPOXIDE HYDROLASE 1, MICROSOMAL; EPHX1 *132811 : EPOXIDE HYDROLASE 2, CYTOSOLIC; EPHX2 132850 : EPSTEIN-BARR VIRUS INSERTION SITE 1; EBVS1 132860 : EPSTEIN-BARR VIRUS MODIFICATION SITE 1; EBVM1 *132880 : NUCLEAR RECEPTOR SUBFAMILY 2, GROUP F, MEMBER 6; NR2F6 *132890 : NUCLEAR RECEPTOR SUBFAMILY 2, GROUP F, MEMBER 1; NR2F1 #132900 : AORTIC ANEURYSM, THORACIC 132990 : ERYTHEMA NODOSUM, FAMILIAL *133000 : ERYTHEMA PALMARE HEREDITARIUM *133020 : ERYTHERMALGIA, FAMILIAL PRIMARY *133090 : ERYTHROCYTE SURFACE PROTEIN BAND 7.2; EPB72 #133100 : ERYTHROCYTOSIS, FAMILIAL *133170 : ERYTHROPOIETIN; EPO *133171 : ERYTHROPOIETIN RECEPTOR; EPOR 133180 : ERYTHROLEUKEMIA, FAMILIAL *133190 : ERYTHROKERATODERMIA WITH ATAXIA #133200 : ERYTHROKERATODERMIA VARIABILIS; EKV *133220 : ESTERASE A-4; ESA4 *133230 : ESTERASE A-5; ESA5 #133239 : ESOPHAGEAL CANCER 133240 : ESOPHAGEAL RING, LOWER *133250 : ESTERASE ACTIVATOR; ESAT 133260 : ESTERASE B; ESB 133270 : ESTERASE C; ESC *133280 : ESTERASE D; ESD *133290 : ESTERASE B3; ESB3 133300 : ESTERASE ES-2, REGULATOR FOR ^133420 : MOVED TO 113710 *133430 : ESTROGEN RECEPTOR 1; ESR1 *133435 : CORE-BINDING FACTOR, ALPHA SUBUNIT 2, TRANSLOCATED TO, 1; CBFA2T1 *133440 : EUKARYOTIC TRANSLATION INITIATION FACTOR 4E; EIF4E *133450 : EWING SARCOMA BREAKPOINT REGION 1; EWSR1 *133500 : EXCHONDROSIS OF PINNA, POSTERIOR *133510 : EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 3; ERCC3 *133520 : EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 4; ERCC4 *133530 : EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 5; ERCC5 *133535 : EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN MOUSE CELLS; ERCM1 *133540 : EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 *133550 : SOLUTE CARRIER FAMILY 1 (NEURONAL/EPITHELIAL HIGH AFFINITY GLUTAMATE TRANSPORTER), MEMBER 1; SLC1A1 133600 : EXOSTOSES OF HEEL 133690 : EXOSTOSES WITH ANETODERMIA AND BRACHYDACTYLY, TYPE E *133700 : EXOSTOSES, MULTIPLE, TYPE I *133701 : EXOSTOSES, MULTIPLE, TYPE II; EXT2 133705 : EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS ^133710 : REMOVED FROM DATABASE ^133730 : REMOVED FROM DATABASE ^133740 : REMOVED FROM DATABASE 133750 : EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATION AND MICROCEPHALY *133780 : EXUDATIVE VITREORETINOPATHY, FAMILIAL; EVR 133800 : EYEBROW, WHORL IN 133900 : FACIAL ASYMMETRY 134000 : FACIAL HYPERTRICHOSIS 134100 : FACIAL PALSY, CONGENITAL UNILATERAL OR BILATERAL *134200 : FACIAL PALSY, FAMILIAL RECURRENT PERIPHERAL 134300 : FACIAL SPASM *134350 : FACTOR D *134370 : H FACTOR 1; HF1 *134371 : FACTOR H-RELATED GENE 1; FHR1 *134390 : FACTOR III, COAGULATION; F3 134400 : FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS 134430 : FACTOR VII AND FACTOR VIII, COMBINED DEFICIENCY OF *134450 : FACTOR VII REGULATOR; F7R 134500 : FACTOR VIII DEFICIENCY 134510 : FACTOR VIII AND FACTOR IX, COMBINED DEFICIENCY OF 134520 : FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF 134530 : FACTOR X, QUANTITATIVE VARIATION IN 134540 : FACTOR IX AND FACTOR XI, COMBINED DEFICIENCY OF *134570 : FACTOR XIII, A1 SUBUNIT; F13A1 *134580 : FACTOR XIII, B SUBUNIT; F13B *134600 : FANCONI RENOTUBULAR SYNDROME *134610 : FAMILIAL MEDITERRANEAN FEVER-LIKE SYNDROME WITH AMYLOIDOSIS, AUTOSOMAL DOMINANT *134629 : FARNESYL DIPHOSPHATE SYNTHASE; FDPS *134631 : FARNESYL DIPHOSPHATE SYNTHASE-LIKE 1; FDPSL1 134632 : FARNESYL DIPHOSPHATE SYNTHASE-LIKE 2; FDPSL2 134633 : FARNESYLPYROPHOSPHATE SYNTHETASE 3; FPSL3 134634 : FARNESYLPYROPHOSPHATE SYNTHETASE 4; FPSL4 *134635 : FARNESYLTRANSFERASE, CAAX BOX, ALPHA; FNTA *134636 : FARNESYLTRANSFERASE, CAAX BOX, BETA; FNTB *134637 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 6; TNFRSF6 *134638 : TUMOR NECROSIS FACTOR LIGAND SUPERFAMILY, MEMBER 6; TNFSF6 *134640 : FATTY ACID-BINDING PROTEIN 2; FABP2 *134650 : FATTY ACID-BINDING PROTEIN 1; FABP1 *134651 : FATTY ACID-BINDING PROTEIN 3; FABP3 *134660 : GLUTATHIONE S-TRANSFERASE, PI; GSTP1 *134690 : FAU GENE; FAU 134700 : FAVISM, SUSCEPTIBILITY TO 134720 : FECUNDITY GENE, BOOROOLA, OF SHEEP, HOMOLOG OF 134750 : FELTY SYNDROME *134770 : FERRITIN HEAVY CHAIN 1; FTH1 134780 : FEMORAL-FACIAL SYNDROME; FFS *134790 : FERRITIN LIGHT CHAIN; FTL *134795 : FIBRILLARIN; FBL *134797 : FIBRILLIN 1; FBN1 *134820 : FIBRINOGEN, A ALPHA POLYPEPTIDE; FGA *134830 : FIBRINOGEN, B BETA POLYPEPTIDE; FGB *134850 : FIBRINOGEN, G GAMMA POLYPEPTIDE; FGG 134900 : FIBRINOLYTIC DEFECT *134920 : FIBROBLAST GROWTH FACTOR 2; FGF2 *134921 : FIBROBLAST GROWTH FACTOR 6; FGF6 *134934 : FIBROBLAST GROWTH FACTOR RECEPTOR 3; FGFR3 *134935 : FIBROBLAST GROWTH FACTOR RECEPTOR 4; FGFR4 *135000 : FIBROCYSTIC PULMONARY DYSPLASIA *135100 : FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP *135150 : BIRT-HOGG-DUBE SYNDROME; BHD #135290 : DESMOID DISEASE, HEREDITARY #135300 : FIBROMATOSIS, GINGIVAL, 1; GINGF 135400 : FIBROMATOSIS, GINGIVAL, WITH HYPERTRICHOSIS *135500 : FIBROMATOSIS, GINGIVAL, WITH ABNORMAL FINGERS, FINGERNAILS, NOSE AND EARS, AND SPLENOMEGALY *135550 : FIBROMATOSIS, GINGIVAL, WITH PROGRESSIVE DEAFNESS 135580 : FIBROMUSCULAR DYSPLASIA OF ARTERIES *135600 : FIBRONECTIN 1; FN1 135610 : FIBRONECTIN-LIKE 2; FNL2 *135620 : INTEGRIN, ALPHA-5; ITGA5 *135630 : INTEGRIN, BETA-1; ITGB1 ^135631 : MOVED TO 135630 *135700 : FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; FEOM1 135750 : FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUS 135800 : FIBULA, RECURRENT DISLOCATION OF HEAD OF *135820 : FIBULIN 1; FBLN1 *135821 : FIBULIN 2; FBLN2 135900 : FIFTH DIGIT SYNDROME *135940 : FILAGGRIN; FLG 135950 : FINGER LOCKING, RECURRENT, WITH INTRAUTERINE GROWTH RETARDATION AND PROPORTIONATE SHORT STATURE *136000 : FINGERPRINTS, ABSENCE OF 136100 : FINGERS, RELATIVE LENGTH OF #136120 : FISH-EYE DISEASE; FED *136130 : FLAVIN-CONTAINING MONOOXYGENASE 1; FMO1 *136131 : FLAVIN-CONTAINING MONOOXYGENASE 4; FMO4 *136132 : FLAVIN-CONTAINING MONOOXYGENASE 3; FMO3 136140 : FLOATING-HARBOR SYNDROME 136150 : FLOOD FACTOR DEFICIENCY 136200 : FLUSHING OF EARS AND SOMNOLENCE *136300 : FLYNN-AIRD SYNDROME *136350 : FIBROBLAST GROWTH FACTOR RECEPTOR 1; FGFR1 *136351 : FMS-RELATED TYROSINE KINASE 3; FLT3 *136352 : FMS-LIKE TYROSINE KINASE 4; FLT4 136400 : FOCAL EPITHELIAL HYPERPLASIA OF THE ORAL MUCOSA *136425 : FOLATE RECEPTOR 2, FETAL; FOLR2 *136430 : FOLATE RECEPTOR 1, ADULT; FOLR1 *136435 : FOLLICLE-STIMULATING HORMONE RECEPTOR; FSHR *136440 : FOLLICULAR-VARIANT-TRANSLOCATION GENE; FVT1 *136470 : FOLLISTATIN; FST 136480 : FOURTH CRANIAL NERVE PALSY, FAMILIAL CONGENITAL *136490 : FORMALDEHYDE DEHYDROGENASE; FDH *136500 : FOCAL FACIAL DERMAL DYSPLASIA *136510 : FOLYLPOLYGLUTAMATE SYNTHETASE; FPGS *136515 : FOS-LIKE ANTIGEN 1; FOSL1 #136520 : FOVEAL HYPOPLASIA AND PRESENILE CATARACT SYNDROME *136530 : FOLLICLE-STIMULATING HORMONE, BETA POLYPEPTIDE; FSHB *136533 : FORKHEAD BOX O1A; FOXO1A *136535 : FORMIN; FMN *136537 : FORMYL PEPTIDE RECEPTOR 1; FPR1 *136538 : FORMYL PEPTIDE RECEPTOR-LIKE 1; FPRL1 *136539 : FORMYL PEPTIDE RECEPTOR-LIKE 2; FPRL2 #136540 : FRAGILE SITE 10q23 *136550 : MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE; MCDR1 #136560 : FRAGILE SITE 11q13 #136570 : FRAGILE SITE 16p12 #136580 : FRAGILE SITE 16q22; FRA16A #136590 : FRAGILE SITE 20p11 136600 : FRIEDREICH ATAXIA, SO-CALLED, WITH OPTIC ATROPHY AND SENSORINEURAL DEAFNESS #136610 : FRAGILE SITE 2q11 #136620 : FRAGILE SITE 10q25 #136630 : FRAGILE SITE, FOLIC ACID TYPE, RARE, fra(12)(q13.1); FRA12A #136640 : FRAGILE SITE 9q32 ^136650 : MOVED TO 601153 #136660 : FRAGILE SITE 17p12 #136670 : FRAGILE SITE: ADDITIONAL TYPES #136680 : FRASIER SYNDROME 136750 : FRIEND MURINE LEUKEMIA VIRUS INTEGRATION SITE 1, MOUSE, HOMOLOG OF; FIM1 136760 : FRONTONASAL DYSPLASIA 136770 : FRIEND MURINE LEUKEMIA VIRUS INTEGRATION SITE 3, MOUSE, HOMOLOG OF; FIM3 #136800 : CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL *136820 : FUCOSIDASE, ALPHA-L, 2; FUCA2 136830 : FUCOSIDASE REGULATOR *136835 : FUCOSYLTRANSFERASE 5; FUT5 *136836 : FUCOSYLTRANSFERASE 6; FUT6 *136840 : FULL-LENGTH RETROVIRAL SEQUENCE 1; FRV1 *136850 : FUMARATE HYDRATASE; FH *136870 : FULL-LENGTH RETROVIRAL SEQUENCE 2; FRV2 #136880 : FUNDUS ALBIPUNCTATUS *136890 : FULL-LENGTH RETROVIRAL SEQUENCE 3; FRV3 #136900 : FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY; SFD *136950 : PAIRED BASIC AMINO ACID CLEAVING ENZYME; PACE 137000 : FUTCHER LINE *137010 : F9 EMBRYONIC ANTIGEN; FEA *137020 : TISSUE-SPECIFIC TRANSPLANTATION ANTIGEN 3; TSTA3 *137025 : FYN ONCOGENE RELATED TO SRC, FGR, YES; FYN *137026 : G PROTEIN-COUPLED RECEPTOR KINASE 2 (DROSOPHILA)-LIKE; GPRK2L *137028 : GALACTOKINASE 2; GALK2 137030 : GALACTOSE + ACTIVATOR; GLAT ^137033 : MOVED TO 153619 *137035 : GALANIN; GAL 137040 : GALLBLADDER, AGENESIS OF 137050 : GAMMA-A-GLOBULIN, DEFECT IN ASSEMBLY OF *137060 : UDP-GAL:BETA-GlcNAc BETA-1,4-GALACTOSYLTRANSFERASE, POLYPEPTIDE 1; B4GALT1 *137061 : GALACTOSYLTRANSFERASE ACTIVATOR; GTA *137070 : FUSION, DERIVED FROM 12-16 TRANSLOCATION, MALIGNANT LIPOSARCOMA; FUS *137100 : IMMUNOGLOBULIN A DEFICIENCY SUSCEPTIBILITY 1; IGAD1 137130 : GASTRIC SNEEZING *137140 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, ALPHA-2; GABRA2 *137141 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, ALPHA-4; GABRA4 *137142 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, ALPHA-5; GABRA5 *137143 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, ALPHA-6; GABRA6 *137150 : 4-@AMINOBUTYRATE AMINOTRANSFERASE; ABAT *137160 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, ALPHA-1; GABRA1 *137161 : GAMMA-AMINOBUTYRIC ACID RECEPTOR SUBUNIT RHO1 *137162 : GAMMA-AMINOBUTYRIC ACID RECEPTOR SUBUNIT RHO2 *137163 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, DELTA; GABRD *137164 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, GAMMA-2; GABRG2 *137165 : SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, GABA), MEMBER 1; SLC6A1 *137166 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, GAMMA-1; GABRG1 *137167 : GAMMA-GLUTAMYL CARBOXYLASE; GGCX *137168 : GAMMA-GLUTAMYLTRANSFERASE-LIKE ACTIVITY1; GGTLA1 *137170 : GAMMA-GLUTAMYLCYCLOTRANSFERASE; GCTG *137181 : GAMMA-GLUTAMYLTRANSFERASE 2; GGT2 *137190 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, BETA-1; GABRB1 *137192 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, BETA-3; GABRB3 137200 : GAMSTORP-WOHLFART SYNDROME *137207 : GLYCOPROTEIN A REPETITIONS PREDOMINANT; GARP 137210 : GASTRIC VOLVULUS, INTRATHORACIC #137215 : GASTRIC CANCER *137216 : ATPase, H+,K+ EXCHANGING, ALPHA SUBUNIT; ATP4A *137217 : ATPase, H+,K+ EXCHANGING, BETA POLYPEPTIDE; ATP4B 137220 : GASTRIC JUICE PEPTIDES *137240 : GASTRIC INHIBITORY POLYPEPTIDE; GIP *137241 : GASTRIC INHIBITORY POLYPEPTIDE RECEPTOR; GIPR 137245 : GASTRIC LYMPHOMA, PRIMARY *137250 : GASTRIN; GAS *137260 : GASTRIN-RELEASING POLYPEPTIDE; GRP 137270 : GASTROCUTANEOUS SYNDROME 137280 : GASTRITIS, FAMILIAL GIANT HYPERTROPHIC *137290 : TUMOR-ASSOCIATED CALCIUM SIGNAL TRANSDUCER 2; TACSTD2 *137295 : GATA-BINDING PROTEIN 2; GATA2 *137350 : GELSOLIN; GSN #137357 : GENITOURINARY DYSPLASIA COMPONENT OF WAGR SYNDROME; GUD 137360 : GENOCHONDROMATOSIS 137370 : GENU VALGUM, ST. HELENA FAMILIAL 137400 : GEOGRAPHIC TONGUE AND FISSURED TONGUE #137440 : GERSTMANN-STRAUSSLER DISEASE; GSD *137500 : GIANT NEUTROPHIL LEUKOCYTES 137550 : GIANT PIGMENTED HAIRY NEVUS; GPHN 137560 : GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA *137570 : SOLUTE CARRIER FAMILY 20, MEMBER 1; SLC20A1 137575 : GIGANTIFORM CEMENTOMA, FAMILIAL *137580 : GILLES DE LA TOURETTE SYNDROME; GTS #137600 : IRIDOGONIODYSGENESIS, TYPE 2; IRID2 137700 : GLAUCOMA WITH ELEVATED EPISCLERAL VENOUS PRESSURE #137750 : GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET; JOAG #137760 : GLAUCOMA, PRIMARY OPEN ANGLE, ADULT-ONSET; POAG 137763 : GLAUCOMA AND SLEEP APNEA 137765 : GLAUCOMA-LENS ECTOPIA-MICROSPHEROPHAKIA-STIFFNESS-SHORTNESS SYNDROME; GEMSS *137780 : GLIAL FIBRILLARY ACIDIC PROTEIN; GFAP *137800 : GLIOMA OF BRAIN 137900 : GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN #137920 : GLOMERULOCYSTIC KIDNEY DISEASE, HYPOPLASTIC TYPE; GCKD 137940 : GLOMERULONEPHRITIS WITH SPARSE HAIR AND TELANGIECTASES 137950 : GLOMERULOPATHY WITH GIANT FIBRILLAR DEPOSITS *137960 : GLOMERULOSCLEROSIS GENE Mpv17, HUMAN HOMOLOG OF #138000 : GLOMUVENOUS MALFORMATIONS; GVM *138030 : GLUCAGON; GCG *138032 : GLUCAGON-LIKE PEPTIDE 1 RECEPTOR; GLP1R *138033 : GLUCAGON RECEPTOR; GCGR ^138035 : MOVED TO 230800 *138040 : GLUCOCORTICOID RECEPTOR; GCCR 138060 : GLUCOCORTICOID RECEPTOR-LIKE 1; GRLL1 138070 : GLUCOGLYCINURIA *138079 : GLUCOKINASE; GCK *138090 : GLUCOSE DEHYDROGENASE; GDH *138100 : HEXOSE-6-PHOSPHATE DEHYDROGENASE; H6PD 138110 : GLUCOSE-6-PHOSPHATE DEHYDROGENASE-LIKE; G6PDL *138120 : HEAT-SHOCK 70-KD PROTEIN 5; HSPA5 *138130 : GLUTAMATE DEHYDROGENASE 1; GLUD1 *138140 : SOLUTE CARRIER FAMILY 2 (FACILITATED GLUCOSE TRANSPORTER), MEMBER 1; SLC2A1 *138150 : GLUTAMATE OXALOACETATE TRANSAMINASE, MITOCHONDRIAL; GOT2 *138160 : SOLUTE CARRIER FAMILY 2 (FACILITATED GLUCOSE TRANSPORTER), MEMBER 2; SLC2A2 *138170 : SOLUTE CARRIER FAMILY 2 (FACILITATED GLUCOSE TRANSPORTER), MEMBER 3; SLC2A3 *138180 : GLUTAMATE OXALOACETATE TRANSAMINASE, SOLUBLE; GOT1 *138190 : SOLUTE CARRIER FAMILY 2 (FACILITATED GLUCOSE TRANSPORTER), MEMBER 4; SLC2A4 *138200 : GLUTAMIC-PYRUVATE TRANSAMINASE; GPT 138210 : GLUTAMATE-PYRUVATE TRANSAMINASE, MITOCHONDRIAL; GPT2 ^138220 : MOVED TO 138200 *138230 : SOLUTE CARRIER FAMILY 2 (FACILITATED GLUCOSE/FRUCTOSE TRANSPORTER), MEMBER 5; SLC2A5 ^138240 : MOVED TO 138170 *138243 : GLUTAMATE RECEPTOR, IONOTROPIC, KAINATE 3; GRIK3 *138244 : GLUTAMATE RECEPTOR, IONOTROPIC, KAINATE 2; GRIK2 *138245 : GLUTAMATE RECEPTOR, IONOTROPIC, KAINATE 1; GRIK1 *138246 : GLUTAMATE RECEPTOR, IONOTROPIC, AMPA 4; GRIA4 *138247 : GLUTAMATE RECEPTOR, IONOTROPIC, AMPA 2; GRIA2 *138248 : GLUTAMATE RECEPTOR, IONOTROPIC, AMPA 1; GRIA1 *138249 : GLUTAMATE RECEPTOR, IONOTROPIC, N-METHYL-D-ASPARTATE, SUBUNIT 1; GRIN1 *138250 : 1-@PYRROLINE-5-CARBOXYLATE SYNTHETASE; PYCS *138251 : GLUTAMATE RECEPTOR, IONOTROPIC, N-METHYL-D-ASPARTATE, ASSOCIATED PROTEIN; GRINA *138252 : GLUTAMATE RECEPTOR, IONOTROPIC, N-METHYL-D-ASPARTATE, SUBUNIT 2B; GRIN2B *138253 : GLUTAMATE RECEPTOR, IONOTROPIC, N-METHYL-D-ASPARTATE, SUBUNIT 2A; GRIN2A *138254 : GLUTAMATE RECEPTOR, IONOTROPIC, N-METHYL-D-ASPARTATE, SUBUNIT 2C; GRIN2C *138270 : GLUTATHIONE S-TRANSFERASE, MU-1-LIKE; GSTM1L *138275 : GLUTAMIC ACID DECARBOXYLASE 2; GAD2 *138276 : GLUTAMIC ACID DECARBOXYLASE 3; GAD3 138277 : GLUTAMIC ACID DECARBOXYLASE, BRAIN, MEMBRANE FORM *138280 : GLUTAMINASE, PHOSPHATE-ACTIVATED; GLS *138290 : GLUTAMATE-AMMONIA LIGASE; GLUL *138292 : GLUTAMINE:FRUCTOSE-6-PHOSPHATE AMIDOTRANSFERASE 1; GFPT1 *138295 : GLUTAMYL-PROLYL-tRNA SYNTHETASE; EPRS *138297 : GLUTAMYL AMINOPEPTIDASE; ENPEP *138300 : GLUTATHIONE REDUCTASE; GSR *138319 : GLUTATHIONE PEROXIDASE 2; GPX2 *138320 : GLUTATHIONE PEROXIDASE; GPX1 *138321 : GLUTATHIONE PEROXIDASE 3; GPX3 *138322 : GLUTATHIONE PEROXIDASE 4; GPX4 *138330 : GLUTATHIONE S-TRANSFERASE, MICROSOMAL, 1; MGST1 *138333 : GLUTATHIONE S-TRANSFERASE, MU-4; GSTM4 ^138335 : MOVED TO 138370 138340 : GLUTATHIONE TRANSFERASE ACTIVITY TOWARD TRANS-STILBENE OXIDE *138350 : GLUTATHIONE S-TRANSFERASE, MU-1; GSTM1 *138359 : GLUTATHIONE S-TRANSFERASE, ALPHA-1; GSTA1 *138360 : GLUTATHIONE S-TRANSFERASE, ALPHA-2; GSTA2 ^138370 : MOVED TO 134660 *138380 : GLUTATHIONE S-TRANSFERASE, MU-2; GSTM2 *138385 : GLUTATHIONE S-TRANSFERASE, MU-5; GSTM5 *138390 : GLUTATHIONE S-TRANSFERASE, MU-3; GSTM3 138391 : GLUTATHIONE S-TRANSFERASE 6 *138400 : GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; GAPD *138420 : GLYCEROL-3-PHOSPHATE DEHYDROGENASE 1; GPD1 *138430 : GLYCEROL-3-PHOSPHATE DEHYDROGENASE 2; GPD2 *138440 : PHOSPHORIBOSYLGLYCINAMIDE FORMYLTRANSFERASE/PHOSPHORIBOSYLGLYCINAMIDE SYNTHETASE/PHOSPHORIBOSYLAMINOIMIDAZOLE SYNTHETASE; GART *138450 : SERINE HYDROXYMETHYLTRANSFERASE, MITOCHONDRIAL; SHMT2 *138470 : PROPERDIN FACTOR B; BF *138480 : GLYCINE AUXOTROPH B, HUMAN COMPLEMENT FOR HAMSTER; GLY B+; GLYB *138491 : GLYCINE RECEPTOR, ALPHA-1 SUBUNIT; GLRA1 *138492 : GLYCINE RECEPTOR, BETA SUBUNIT; GLRB 138500 : GLYCINURIA WITH OR WITHOUT OXALATE UROLITHIASIS *138550 : GLYCOGEN PHOSPHORYLASE, BRAIN TYPE; PYGB *138570 : GLYCOGEN SYNTHASE 1; GYS1 *138571 : GLYCOGEN SYNTHASE 2; GYS2 *138590 : GLYCOPHORIN E; GYPE *138600 : OROSOMUCOID 1; ORM1 *138610 : OROSOMUCOID 2; ORM2 *138670 : ALPHA-1-B-GLYCOPROTEIN; A1BG *138680 : ALPHA-2-HS-GLYCOPROTEIN; AHSG *138700 : APOLIPOPROTEIN H; APOH 138710 : GLYCOPROTEIN, RENAL *138720 : GLYCOPROTEIN Ib, PLATELET, BETA POLYPEPTIDE; GP1BB *138750 : GLYOXALASE I; GLO1 *138760 : HYDROXYACYL GLUTATHIONE HYDROLASE; HAGH 138770 : GMS SYNDROME 138790 : GOITER, MULTINODULAR, CYSTIC RENAL DISEASE AND DIGITAL ANOMALIES *138800 : GOITER, MULTINODULAR 1; MNG1 *138850 : GONADOTROPIN-RELEASING HORMONE RECEPTOR; GNRHR *138890 : GOOSECOID; GSC 138900 : GOUT 138920 : GRANDDAD SYNDROME 138930 : GRANT SYNDROME *138945 : GRANULIN; GRN *138960 : COLONY-STIMULATING FACTOR 2; CSF2 *138965 : SMALL INDUCIBLE CYTOKINE SUBFAMILY B, MEMBER 6; SCYB6 *138970 : COLONY-STIMULATING FACTOR 3; CSF3 *138971 : COLONY-STIMULATING FACTOR 3 RECEPTOR, GRANULOCYTE; CSF3R 138972 : CCAAT/ENHANCER-BINDING PROTEIN, GAMMA; CEBPG *138981 : GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR RECEPTOR, BETA; CSF2RB 138990 : GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL DOMINANT TYPE 139000 : GRANULOSIS RUBRA NASI *139080 : SOLUTE CARRIER FAMILY 25, MEMBER 16; SLC25A16 *139090 : GRAY PLATELET SYNDROME; GPS *139100 : GRAYING OF HAIR, PRECOCIOUS *139110 : GRO2 ONCOGENE; GRO2 *139111 : GRO3 ONCOGENE; GRO3 *139130 : GUANINE NUCLEOTIDE-BINDING PROTEIN, BETA-3; GNB3 *139139 : NUCLEAR RECEPTOR SUBFAMILY 4, GROUP A, MEMBER 1; NR4A1 ^139145 : MOVED TO 139139 *139150 : RAS p21 PROTEIN ACTIVATOR 1; RASA1 *139160 : GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA Z POLYPEPTIDE; GNAZ *139180 : GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-INHIBITING, POLYPEPTIDE-h; GNAIH *139185 : GROWTH ARREST-SPECIFIC 1; GAS1 *139190 : GROWTH HORMONE-RELEASING HORMONE; GHRH *139191 : GROWTH HORMONE-RELEASING HORMONE RECEPTOR; GHRHR *139200 : GROUP-SPECIFIC COMPONENT; GC 139210 : GROWTH-MENTAL DEFICIENCY SYNDROME OF MYHRE *139220 : GROWTH-RATE-CONTROLLING FACTOR 1; GCF1 *139230 : GROWTH-RATE-CONTROLLING FACTOR 2; GCF2 *139240 : GROWTH HORMONE 2; GH2 *139250 : GROWTH HORMONE 1; GH1 *139255 : METALLOTHIONEIN 3; MT3 *139259 : G1-TO-S PHASE TRANSITION 1; GSPT1 *139260 : GUANINE DEAMINASE; GDA *139265 : GUANINE MONOPHOSPHATE REDUCTASE *139270 : GUANYLATE KINASE 1; GUK1 139280 : GUANYLATE KINASE 2; GUK2 *139290 : GUANYLATE KINASE 3; GUK3 139300 : GYNECOMASTIA, HEREDITARY *139310 : GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-INHIBITING ACTIVITY POLYPEPTIDE 1; GNAI1 *139311 : GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-ACTIVATING ACTIVITY POLYPEPTIDE O; GNAO1 *139312 : GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-ACTIVATING ACTIVITY POLYPEPTIDE, OLFACTORY TYPE; GNAL *139313 : GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-11; GNA11 *139314 : GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-15; GNA15 *139320 : GNAS COMPLEX LOCUS; GNAS *139330 : GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-TRANSDUCING ACTIVITY POLYPEPTIDE 1; GNAT1 *139340 : GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-TRANSDUCING ACTIVITY POLYPEPTIDE 2; GNAT2 *139350 : KERATIN 1; KRT1 *139360 : GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-INHIBITING ACTIVITY POLYPEPTIDE 2; GNAI2 *139370 : GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-INHIBITING ACTIVITY POLYPEPTIDE 3; GNAI3 *139380 : GUANINE NUCLEOTIDE-BINDING PROTEIN, BETA-1; GNB1 *139390 : GUANINE NUCLEOTIDE-BINDING PROTEIN, BETA-2; GNB2 *139391 : GUANINE NUCLEOTIDE-BINDING PROTEIN, GAMMA-TRANSDUCING, 2 *139392 : GUANYLATE CYCLASE ACTIVATOR 2A; GUCA2A 139393 : GUILLAIN-BARRE SYNDROME, FAMILIAL *139395 : GUSTDUCIN, ALPHA POLYPEPTIDE *139396 : GUANYLATE CYCLASE 1, SOLUBLE, ALPHA-3; GUCY1A3 *139397 : GUANYLATE CYCLASE 1, SOLUBLE, BETA-3; GUCY1B3 139400 : HAIR WHORL 139450 : HAIR, CURLY 139500 : HAIRY EARS 139600 : HAIRY ELBOWS *139605 : 'HAIRY,' DROSOPHILA, HOMOLOG OF; HRY 139630 : HAIRY NOSE TIP *139650 : HAIRY PALMS AND SOLES 139750 : HAND AND FOOT DEFORMITY WITH FLAT FACIES 139800 : HAND CLASPING PATTERN 139900 : HANDEDNESS #140000 : HAND-FOOT-UTERUS SYNDROME *140050 : GRANZYME A; GZMA ^140090 : MOVED TO 189903 *140100 : HAPTOGLOBIN; HP *140210 : HAPTOGLOBIN-RELATED PROTEIN GENE; HPR *140300 : HASHIMOTO STRUMA #140340 : HAW RIVER SYNDROME *140350 : HAWKINSINURIA 140400 : PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II 140450 : HEART-HAND SYNDROME, SPANISH TYPE 140500 : HEART, MALFORMATION OF *140550 : HEAT-SHOCK 70-KD PROTEIN 1A; HSPA1A *140555 : HEAT-SHOCK 70-KD PROTEIN 6; HSPA6 *140556 : HEAT-SHOCK 70-KD PROTEIN 7; HSPA7 *140559 : HEAT-SHOCK 70-KD PROTEIN-LIKE 1; HSPA1L *140560 : HEAT-SHOCK 70-KD PROTEIN 2; HSPA2 *140570 : HEAT-SHOCK 70-KD PROTEIN 3; HSPA3 *140571 : HEAT-SHOCK 90-KD PROTEIN 1, ALPHA; HSPCA *140572 : HEAT-SHOCK 90-KD PROTEIN 1, BETA; HSPCB *140573 : HEAT-SHOCK 90-KD PROTEIN 1, ALPHA-LIKE 1; HSPCAL1 *140574 : HEAT-SHOCK 90-KD PROTEIN 1, ALPHA-LIKE 2; HSPCAL2 *140575 : HEAT-SHOCK 90-KD PROTEIN 1, ALPHA-LIKE 3; HSPCAL3 *140576 : HEAT-SHOCK 90-KD PROTEIN 1, ALPHA-LIKE 4; HSPCAL4 *140580 : HEAT-SHOCK TRANSCRIPTION FACTOR 1; HSF1 *140581 : HEAT-SHOCK TRANSCRIPTION FACTOR 2; HSF2 140600 : OSTEOARTHRITIS OF DISTAL INTERPHALANGEAL JOINTS #140700 : HEINZ BODY ANEMIAS *140750 : SUPPRESSOR OF TUMORIGENICITY 5; ST5 140850 : HEMANGIOMAS, CAVERNOUS, OF FACE AND SUPRAUMBILICAL MIDLINE RAPHE 140900 : HEMANGIOMAS OF SMALL INTESTINE 141000 : HEMANGIOMA-THROMBOCYTOPENIA SYNDROME *141180 : HEMATOPOIETIC PROTEIN HEM-1; HEM1 #141200 : HEMATURIA, BENIGN FAMILIAL; BFH *141250 : HEME OXYGENASE 1; HMOX1 *141251 : HEME OXYGENASE 2; HMOX2 141300 : HEMIFACIAL ATROPHY, PROGRESSIVE; HFA *141350 : HEMIFACIAL HYPERPLASIA WITH STRABISMUS; HFH 141400 : HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS 141405 : HEMIFACIAL SPASM, FAMILIAL #141500 : MIGRAINE, FAMILIAL HEMIPLEGIC, 1; MHP1 141700 : HEMOLYTIC POIKILOCYTIC ANEMIA DUE TO REDUCED ANKYRIN BINDING SITES #141749 : HEMOGLOBIN F, HEREDITARY PERSISTENCE OF, PANCELLULAR #141750 : HEMOGLOBIN H-RELATED MENTAL RETARDATION *141800 : HEMOGLOBIN--ALPHA LOCUS 1; HBA1 *141850 : HEMOGLOBIN--ALPHA LOCUS 2; HBA2 *141860 : HEMOGLOBIN--ALPHA LOCUS 3 *141900 : HEMOGLOBIN--BETA LOCUS; HBB ^141940 : MOVED TO 141900 *142000 : HEMOGLOBIN--DELTA LOCUS; HBD *142100 : HEMOGLOBIN--EPSILON LOCUS; HBE1 *142200 : HEMOGLOBIN, GAMMA A; HBG1 *142210 : H1 HISTONE FAMILY, MEMBER 3; H1F3 *142220 : H1 HISTONE FAMILY, MEMBER 4; H1F4 *142230 : HEMATOPOIETIC PROGENITOR CELL ANTIGEN CD34; CD34 *142240 : HEMOGLOBIN--THETA-1 LOCUS; HBQ1 *142250 : HEMOGLOBIN, GAMMA G; HBG2 ^142270 : MOVED TO 142200 *142290 : HEMOPEXIN; HPX ^142300 : MOVED TO 142310 #142309 : HEMOGLOBIN--VARIANTS FOR WHICH THE CHAIN CARRYING THE MUTATION IS UNKNOWN OR UNCERTAIN *142310 : HEMOGLOBIN--ZETA LOCUS; HBZ 142330 : HEPATIC ADENOMAS, FAMILIAL ^142333 : MOVED TO 114550 *142335 : HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, HETEROCELLULAR, INDIAN TYPE; HPFH2 142340 : HERNIA, DIAPHRAGMATIC 142350 : HERNIA, DOUBLE INGUINAL *142360 : HEPARIN COFACTOR II; HCF2 *142370 : HEMOPOIETIC CELL KINASE; HCK ^142380 : MOVED TO 114550 *142385 : HEPATIC LEUKEMIA FACTOR; HLF *142390 : HEPATIC PROTEIN; HEP10 142395 : HEPATITIS B VACCINE, RESPONSE TO *142400 : HERNIA, HIATUS *142408 : MACROPHAGE STIMULATING 1; MST1 *142409 : HEPATOCYTE GROWTH FACTOR; HGF *142410 : TRANSCRIPTION FACTOR 1; TCF1 ^142420 : REMOVED FROM DATABASE *142440 : HEPSIN; HPN *142445 : NEUREGULIN 1; NRG1 *142450 : HERPESVIRUS SENSITIVITY; HV1S *142460 : SYNDECAN 2; SDC2 *142461 : HEPARAN SULFATE PROTEOGLYCAN OF BASEMENT MEMBRANE; HSPG2 *142470 : HETEROCELLULAR HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN 142500 : HETEROCHROMIA IRIDIS ^142510 : MOVED TO 300049 142550 : HEXOKINASE OF SPERMATOZOA *142560 : HLA-B-ASSOCIATED TRANSCRIPT 1; BAT1 *142570 : HEXOKINASE 3; HK3 *142580 : HLA-B-ASSOCIATED TRANSCRIPT 2; BAT2 *142590 : HLA-B-ASSOCIATED TRANSCRIPT 3; BAT3 *142600 : HEXOKINASE 1; HK1 *142610 : HLA-B-ASSOCIATED TRANSCRIPT 4; BAT4 *142620 : HLA-B-ASSOCIATED TRANSCRIPT 5; BAT5 *142622 : HIPPOCALCIN; HPCA #142623 : HIRSCHSPRUNG DISEASE 142625 : HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME 142630 : HISTIOCYTOSIS, PROGRESSIVE MUCINOUS *142640 : HISTIDINE-RICH GLYCOPROTEIN; HRG *142660 : HEXOSAMINIDASE C; HEXC *142669 : HIP DYSPLASIA, BEUKES TYPE #142680 : PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT 142690 : HIDRADENITIS SUPPURATIVA, FAMILIAL *142695 : HIGH DENSITY LIPOPROTEIN-BINDING PROTEIN; HDLBP 142700 : HIP, DISLOCATION OF, CONGENITAL *142701 : HISTATIN 1; HTN1 *142702 : HISTATIN 3; HTN3 *142703 : HISTAMINE RECEPTOR H2; HRH2 *142704 : HISTIDINE DECARBOXYLASE; HDC *142705 : HISTIDINE-RICH CALCIUM-BINDING PROTEIN; HRC *142708 : H1 HISTONE FAMILY, MEMBER 0; H1F0 *142709 : H1 HISTONE FAMILY, MEMBER 1; H1F1 *142710 : H1 HISTONE FAMILY, MEMBER 2; H1F2 *142711 : H1 HISTONE FAMILY, MEMBER 5; H1F5 *142712 : H1 HISTONE FAMILY, MEMBER T; H1FT *142720 : HISTONE 2A FAMILY, MEMBER O; H2AFO 142730 : HISTIOCYTIC DERMATOARTHRITIS *142750 : H4 HISTONE, FAMILY 2; H4F2 ^142760 : MOVED TO 142720 *142763 : H2AZ HISTONE; H2AZ *142765 : REGULATORY FACTOR X, 2; RFX2 142770 : HLA MODIFIER *142780 : H3 HISTONE, FAMILY 2; H3F2 *142790 : CD74 ANTIGEN; CD74 *142795 : HLA-8 HISTOCOMPATIBILITY TYPE; HLA8 *142800 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, A; HLA-A *142810 : HISTIDYL-tRNA SYNTHETASE; HARS *142830 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, B; HLA-B *142840 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, C; HLA-C *142850 : HLA-D HISTOCOMPATIBILITY TYPE *142855 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DM ALPHA; HLA-DMA *142856 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DM BETA; HLA-DMB *142857 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DR BETA-1; HLA-DRB1 *142858 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DP BETA-1; HLA-DPB1 *142860 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DR ALPHA; HLA-DRA ^142870 : REMOVED FROM DATABASE *142871 : HLA-G HISTOCOMPATIBILITY ANTIGEN, CLASS I; HLA-G *142880 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DP ALPHA-1; HLA-DPA1 *142890 : HLA-MT HISTOCOMPATIBILITY TYPE; HLA-MT #142900 : HOLT-ORAM SYNDROME; HOS *142910 : 3-@HYDROXY-3-METHYLGLUTARYL-CoA REDUCTASE; HMGCR *142920 : HLA-DO HISTOCOMPATIBILITY TYPE; HLA-DO ^142925 : MOVED TO 142800 *142930 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DN ALPHA; HLA-DNA *142940 : 3-@HYDROXY-3-METHYLGLUTARYL-CoA SYNTHASE 1, SOLUBLE; HMGCS1 #142945 : HOLOPROSENCEPHALY 3; HPE3 #142946 : HOLOPROSENCEPHALY 4; HPE4 *142950 : HOMEO BOX A7; HOXA7 *142951 : HOMEO BOX A6; HOXA6 *142952 : HOMEO BOX A5; HOXA5 *142953 : HOMEO BOX A4; HOXA4 *142954 : HOMEO BOX A3; HOXA3 *142955 : HOMEO BOX A1; HOXA1 *142956 : HOMEO BOX A9; HOXA9 *142957 : HOMEO BOX A10; HOXA10 *142958 : HOMEO BOX A11; HOXA11 *142959 : HOMEO BOX A13; HOXA13 *142960 : HOMEO BOX B5; HOXB5 *142961 : HOMEO BOX B6; HOXB6 *142962 : HOMEO BOX B7; HOXB7 *142963 : HOMEO BOX B8; HOXB8 *142964 : HOMEO BOX B9; HOXB9 *142965 : HOMEO BOX B4; HOXB4 *142966 : HOMEO BOX B3; HOXB3 *142967 : HOMEO BOX B2; HOXB2 *142968 : HOMEO BOX B1; HOXB1 *142970 : HOMEO BOX C8; HOXC8 *142971 : HOMEO BOX C9; HOXC9 *142972 : HOMEO BOX C6; HOXC6 *142973 : HOMEO BOX 3D; HOX3D *142974 : HOMEO BOX C4; HOXC4 *142975 : HOMEO BOX 3F; HOX3F *142976 : HOMEO BOX C13; HOXC13 *142980 : HOMEO BOX D3; HOXD3 *142981 : HOMEO BOX D4; HOXD4 *142982 : HOMEO BOX D9; HOXD9 *142983 : MUSCLE SEGMENT HOMEO BOX, DROSOPHILA, HOMOLOG OF, 1; MSX1 *142984 : HOMEO BOX D10; HOXD10 *142985 : HOMEO BOX D8; HOXD8 *142986 : HOMEO BOX D11; HOXD11 *142987 : HOMEO BOX D1; HOXD1 *142988 : HOMEO BOX D12; HOXD12 *142989 : HOMEO BOX D13; HOXD13 ^142990 : MOVED TO 142981 *142991 : EVEN-SKIPPED HOMEO BOX 2; EVX2 *142992 : HOMEO BOX (H6 FAMILY) 1; HMX1 *142993 : CEH10 HOMEODOMAIN-CONTAINING HOMOLOG; CHX10 *142994 : HOMEO BOX GENE HB9; HLXB9 *142995 : HOMEO BOX GENE HB24 *142996 : EVEN-SKIPPED HOMEO BOX 1; EVX1 *143000 : HORNER SYNDROME *143010 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, E; HLA-E #143020 : HPA I RECOGNITION POLYMORPHISM, BETA-GLOBIN-RELATED; HPA1 *143023 : CHROMOSOME 11 OPEN READING FRAME 13; C11ORF13 *143024 : GUANINE NUCLEOTIDE-BINDING PROTEIN-LIKE 1; GNL1 *143025 : HTLV-RELATED ENDOGENOUS SEQUENCE 1; HRES1 *143030 : CD9 ANTIGEN; CD9 *143040 : ANTIGEN DEFINED BY MONOCLONAL ANTIBODY F10.44.2 143050 : HUMERORADIAL SYNOSTOSIS *143054 : HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 ENHANCER-BINDING PROTEIN 2; HIVEP2 *143055 : HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 EXPRESSION 1; HIVE1 *143060 : HUMAN LEUKOCYTE ANTIGEN MIC6; MIC6 ^143065 : MOVED TO 107271 ^143070 : REMOVED FROM DATABASE ^143080 : REMOVED FROM DATABASE *143089 : HUMAN T-CELL LEUKEMIA VIRUS ENHANCER FACTOR; HTLF *143090 : HUMAN T-CELL LEUKEMIA VIRUS RECEPTOR; HTLVR 143095 : HUMEROSPINAL DYSOSTOSIS *143100 : HUNTINGTON DISEASE; HD *143110 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, F; HLA-F 143150 : H-Y ANTIGEN RECEPTOR *143170 : MALE-ENHANCED ANTIGEN; MEA *143200 : HYALOIDEORETINAL DEGENERATION OF WAGNER *143400 : MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MRD *143450 : HYDROXYACYL-CoA DEHYDROGENASE/3-KETOACYL-CoA THIOLASE/ENOYL-CoA HYDRATASE, BETA SUBUNIT; HADHB 143460 : 5-@HYDROXYTRYPTAMINE OXYGENASE REGULATOR; HTOR 143465 : ATTENTION DEFICIT-HYPERACTIVITY DISORDER; ADHD 143470 : HYPERALPHALIPOPROTEINEMIA #143500 : GILBERT SYNDROME *143850 : ORTHOSTATIC HYPOTENSIVE DISORDER, STREETEN TYPE 143860 : HYPERCHLORHIDROSIS, ISOLATED *143870 : HYPERCALCIURIA, ABSORPTIVE, 1 143880 : HYPERCALCEMIA, IDIOPATHIC, OF INFANCY #143890 : HYPERCHOLESTEROLEMIA, FAMILIAL #144010 : HYPERCHOLESTEROLEMIA, FAMILIAL, TYPE B 144020 : HYPERCHOLESTEROLEMIA SUPPRESSOR 144050 : HYPERHEPARINEMIA 144100 : HYPERHIDROSIS, GUSTATORY 144110 : HYPERHIDROSIS PALMARIS ET PLANTARIS 144120 : HYPERIMMUNOGLOBULIN G1(A1) SYNDROME *144150 : HYPERKERATOSIS LENTICULARIS PERSTANS; HLP 144190 : HYPERKERATOSIS-HYPERPIGMENTATION SYNDROME *144200 : HYPERKERATOSIS, LOCALIZED EPIDERMOLYTIC #144250 : HYPERLIPIDEMIA, FAMILIAL COMBINED 144300 : HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS #144400 : HYPERLIPOPROTEINEMIA, TYPE II 144600 : HYPERLIPOPROTEINEMIA, TYPE IV 144650 : HYPERLIPOPROTEINEMIA, TYPE V #144700 : RENAL CELL CARCINOMA 1; RCC1 *144750 : HYPEROSTOSIS CORTICALIS GENERALISATA, BENIGN FORM OF WORTH, WITH TORUS PALATINUS 144755 : HYPEROSTOSIS CRANIALIS INTERNA 144800 : HYPEROSTOSIS FRONTALIS INTERNA #145000 : HYPERPARATHYROIDISM 1; HRPT1 *145001 : HYPERPARATHYROIDISM 2; HRPT2 *145100 : HYPERPIGMENTATION OF EYELIDS 145200 : HYPERPIGMENTATION OF FULDAUER AND KUIJPERS *145250 : HYPERPIGMENTATION, FAMILIAL PROGRESSIVE #145260 : PSEUDOHYPOALDOSTERONISM, TYPE II; PHA2 145270 : HYPERPROGLUCAGONEMIA 145290 : HYPERREFLEXIA; HRX 145295 : HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL 145300 : HYPERSENSITIVITY PNEUMONITIS, FAMILIAL 145350 : HYPERTAURINURIC CARDIOMYOPATHY *145400 : HYPERTELORISM *145410 : HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS *145420 : HYPERTELORISM, TEEBI TYPE #145500 : HYPERTENSION, ESSENTIAL *145505 : HYPERTENSION-ASSOCIATED SA, RAT, HOMOLOG OF; SAH 145590 : HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA #145600 : MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 1; MHS1 #145650 : HYPERTHYROIDISM, FAMILIAL, DUE TO INAPPROPRIATE THYROTROPIN SECRETION *145680 : HYPERTHYROXINEMIA, FAMILIAL *145700 : HYPERTRICHOSIS UNIVERSALIS *145701 : HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE; HTC1 *145750 : HYPERTRIGLYCERIDEMIA, FAMILIAL *145800 : HYPERTROPHIA MUSCULORUM VERA #145900 : HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS #145980 : HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I; HHC1 *145981 : HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II; HHC2 #146000 : HYPOCHONDROPLASIA; HCH #146110 : HYPOGONADOTROPIC HYPOGONADISM ^146150 : MOVED TO 300337 146160 : HYPOMELIA WITH MULLERIAN DUCT ANOMALIES #146200 : HYPOPARATHYROIDISM, FAMILIAL ISOLATED; FIH #146255 : HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DYSPLASIA #146300 : HYPOPHOSPHATASIA, ADULT TYPE 146350 : HYPOPHOSPHATEMIC BONE DISEASE; HBD 146390 : HYPOPITUITARISM ASSOCIATED WITH 18p- SYNDROME 146400 : HYPOPLASIA OF TEETH ROOTS 146450 : HYPOSPADIAS 146500 : HYPOTENSION, ORTHOSTATIC #146510 : PALLISTER-HALL SYNDROME; PHS *146520 : HYPOTRICHOSIS SIMPLEX OF SCALP *146530 : HYPOTRICHOSIS WITH LIGHT-COLORED HAIR AND FACIAL MILIA *146550 : HYPOTRICHOSIS, MARIE UNNA TYPE 146580 : HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE SUPPRESSOR *146590 : ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE; IHCM 146600 : ICHTHYOSIS HYSTRIX GRAVIOR *146630 : INTERCELLULAR ADHESION MOLECULE 2; ICAM2 *146631 : INTERCELLULAR ADHESION MOLECULE 3; ICAM3 *146640 : INTER-ALPHA-TRYPSIN INHIBITOR, HEAVY CHAIN 2; ITIH2 *146650 : INTER-ALPHA-TRYPSIN INHIBITOR, HEAVY CHAIN 3; ITIH3 *146660 : INTERLEUKIN 7; IL7 *146661 : INTERLEUKIN 7 RECEPTOR; IL7R *146680 : INSULIN-DEGRADING ENZYME; IDE *146690 : IMP DEHYDROGENASE 1; IMPDH1 *146691 : IMP DEHYDROGENASE 2; IMPDH2 ^146692 : MOVED TO 146690 *146700 : ICHTHYOSIS VULGARIS *146710 : INTERLEUKIN 2 RECEPTOR, BETA; IL2RB 146720 : ICHTHYOSIS--CHEEK--EYEBROW SYNDROME *146730 : INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN 1; IGFBP1 *146731 : INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN 2; IGFBP2 *146732 : INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN 3; IGFBP3 *146733 : INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN 4; IGFBP4 *146734 : INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN 5; IGFBP5 *146735 : INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN 6; IGFBP6 *146738 : INSULIN-LIKE 3; INSL3 *146740 : Fc FRAGMENT OF IgG, LOW AFFINITY IIIa, RECEPTOR FOR; FCGR3A 146750 : ICHTHYOSIS, LAMELLAR, AUTOSOMAL DOMINANT FORM *146760 : Fc FRAGMENT OF IgG, HIGH AFFINITY Ia, RECEPTOR FOR; FCGR1A *146770 : IMMUNOGLOBULIN LAMBDA-LIKE POLYPEPTIDE 1; IGLL1 ^146771 : MOVED TO 146770 *146780 : IMMUNOGLOBULIN KAPPA DELETING ELEMENT; IGKDEL *146790 : Fc FRAGMENT OF IgG, LOW AFFINITY IIa, RECEPTOR FOR; FCGR2A #146800 : ICHTHYOSIS, BULLOUS TYPE *146810 : IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRPHEGAL; IPHEG *146820 : IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRGAT; IGAT 146830 : IMMUNE DEFICIENCY, FAMILIAL VARIABLE 146840 : IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST 146850 : IMMUNE SUPPRESSION; IS *146880 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DQ ALPHA-1; HLA-DQA1 *146900 : IgA CONSTANT HEAVY CHAIN 1; IGHA1 *146910 : IMMUNOGLOBULIN: D (DIVERSITY) REGION OF HEAVY CHAIN *146920 : INTERFERON-INDUCED PROTEIN 4; IFI4 *146928 : INTERLEUKIN 8 RECEPTOR, BETA; IL8RB *146929 : INTERLEUKIN 8 RECEPTOR, ALPHA; IL8RA *146930 : INTERLEUKIN 8; IL8 *146931 : INTERLEUKIN 9; IL9 ^146932 : MOVED TO 300007 *146933 : INTERLEUKIN 10 RECEPTOR, ALPHA; IL10RA ^146940 : MOVED TO 147220 *146950 : IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRHGAL; IHG *146960 : IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRTGAL; ITG *146970 : IMMUNOGLOBULIN: J REGION GENES OF KAPPA LIGHT CHAIN; IGKJ *146980 : IMMUNOGLOBULIN: VARIABLE REGION GENES OF KAPPA LIGHT CHAIN; IGKV 146990 : IMMUNOGLOBULIN HEAVY CHAIN DIVERSITY REGION 2; IGHDY2 *147000 : IgA CONSTANT HEAVY CHAIN 2; IGHA2 *147010 : IMMUNOGLOBULIN: J (JOINING) LOCI OF HEAVY CHAIN; IGHJ *147020 : IMMUNOGLOBULIN MU; IGHM *147040 : INTERFERON-INDUCED PROTEIN WITH TETRATRICOPEPTIDE REPEATS 2; IFIT2 *147045 : Fc FRAGMENT OF IgA, RECEPTOR FOR; FCAR *147050 : IgE RESPONSIVENESS, ATOPIC; IGER *147060 : HYPER-IgE SYNDROME *147061 : IMMUNOGLOBULIN E CONCENTRATION, SERUM; IGES *147070 : IMMUNOGLOBULIN HEAVY VARIABLE CLUSTER; IGHV *147080 : IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRGLPHE 1; IGLP1 *147090 : IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRGLPHE 2; IGLP2 *147100 : IgG HEAVY CHAIN LOCUS; IGHG1 *147110 : IMMUNOGLOBULIN Gm2; IGHG2 *147120 : IMMUNOGLOBULIN Gm3; IGHG3 *147130 : IMMUNOGLOBULIN Gm4; IGHG4 *147138 : MEMBRANE-SPANNING 4 DOMAINS, SUBFAMILY A, MEMBER 2; MS4A2 *147139 : Fc FRAGMENT OF IgE, HIGH AFFINITY I, RECEPTOR FOR, GAMMA SUBUNIT; FCER1G *147140 : Fc FRAGMENT OF IgE, HIGH AFFINITY I, RECEPTOR FOR, ALPHA SUBUNIT; FCER1A *147141 : TRANSCRIPTION FACTOR 3; TCF3 *147150 : MYXOVIRUS RESISTANCE 1, MOUSE, HOMOLOG OF; MX1 ^147160 : MOVED TO 147180 *147170 : IMMUNOGLOBULIN: HEAVY DELTA CHAIN; IGHD *147180 : IMMUNOGLOBULIN: HEAVY EPSILON CHAIN; IGHE *147183 : RECOMBINATION SIGNAL-BINDING PROTEIN SUPPRESSOR OF HAIRLESS, DROSOPHILA, HOMOLOG OF; RBPSUH *147185 : IMMUNOGLOBULIN KAPPA VARIABLE 1/OR2-108; IGKV1OR2108 *147200 : IMMUNOGLOBULIN KAPPA CONSTANT REGION; IGKC ^147210 : MOVED TO 147180 *147220 : IMMUNOGLOBULIN LAMBDA CONSTANT REGION 1; IGLC1 *147230 : IMMUNOGLOBULIN: LAMBDA LIGHT CHAIN, J REGION GENES; IGLJ *147240 : IMMUNOGLOBULIN: LAMBDA LIGHT CHAIN, VARIABLE REGION GENES; IGLV *147245 : CD79B ANTIGEN; CD79B #147250 : SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI 147251 : INCISORS, FUSED MANDIBULAR 147260 : IMMUNOGLOBULIN SWITCH SEQUENCES *147263 : INOSITOL POLYPHOSPHATE-1-PHOSPHATASE; INPP1 *147264 : INOSITOL POLYPHOSPHATE-5-PHOSPHATASE, 75-KD; INPP5B *147265 : INOSITOL 1,4,5-TRIPHOSPHATE RECEPTOR, TYPE 1; ITPR1 *147267 : INOSITOL 1,4,5-TRIPHOSPHATE RECEPTOR, TYPE 3; ITPR3 *147270 : INTER-ALPHA-TRYPSIN INHIBITOR, HEAVY CHAIN 1; ITIH1 *147280 : INSULIN-LIKE GROWTH FACTOR II RECEPTOR; IGF2R *147290 : INHIBIN, BETA A; INHBA 147300 : INCISORS, LONG UPPER CENTRAL *147310 : SMALL INDUCIBLE CYTOKINE SUBFAMILY B, MEMBER 10; SCYB10 147320 : INSULIN RECEPTORS, FAMILIAL INCREASE IN 147330 : INCISORS, LOWER CENTRAL, ABSENCE OF 147350 : INCISORS, ROTATION OF UPPER CENTRAL *147360 : INVOLUCRIN; IVL *147370 : INSULIN-LIKE GROWTH FACTOR I RECEPTOR; IGF1R *147380 : INHIBIN, ALPHA; INHA *147390 : INHIBIN, BETA B; INHBB 147400 : INCISORS, SHOVEL-SHAPED ^147410 : REMOVED FROM DATABASE *147420 : INCLUSION BODY MYOPATHY 147421 : INCLUSION BODY MYOSITIS 147430 : INDIFFERENCE TO PAIN *147435 : INDOLEAMINE 2,3-DIOXYGENASE; INDO *147440 : INSULIN-LIKE GROWTH FACTOR I; IGF1 *147450 : SUPEROXIDE DISMUTASE 1; SOD1 *147460 : SUPEROXIDE DISMUTASE 2; SOD2 *147470 : INSULIN-LIKE GROWTH FACTOR II; IGF2 #147480 : CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY; ICP *147485 : INTRACISTERNAL A PARTICLE-PROMOTED POLYPEPTIDE; IPP *147490 : INSULIN-LIKE DNA SEQUENCE; INSL *147510 : INSULIN-RELATED DNA POLYMORPHISM; IRDN *147520 : INOSINE TRIPHOSPHATASE; ITPA *147521 : INOSITOL 1,4,5-TRISPHOSPHATE 3-KINASE A; ITPKA *147522 : INOSITOL 1,4,5-TRISPHOSPHATE 3-KINASE B; ITPKB 147530 : INSENSITIVITY TO PAIN WITH HYPERPLASTIC MYELINOPATHY 147540 : INSECT STINGS, HYPERSENSITIVITY TO *147545 : INSULIN RECEPTOR SUBSTRATE 1; IRS1 *147553 : INTERFERON, OMEGA-1; IFNW1 ^147554 : MOVED TO 147553 *147556 : INTEGRIN, ALPHA-6; ITGA6 *147557 : INTEGRIN, BETA-4; ITGB4 *147558 : INTEGRIN, BETA-6; ITGB6 *147559 : INTEGRIN, BETA-7; ITGB7 147560 : INTERFERON ANTIVIRAL DEPRESSOR *147561 : INTEGRIN, BETA-5; ITGB5 *147562 : INTERFERON, ALPHA-2; IFNA2 *147563 : INTEGRIN-BINDING SIALOPROTEIN; IBSP *147564 : INTERFERON, ALPHA-4; IFNA4 *147565 : INTERFERON, ALPHA-5; IFNA5 *147566 : INTERFERON, ALPHA-6; IFNA6 *147567 : INTERFERON, ALPHA-7; IFNA7 *147568 : INTERFERON, ALPHA-8; IFNA8 *147569 : INTERFERON, GAMMA, RECEPTOR 2; IFNGR2 *147570 : INTERFERON, GAMMA; IFNG *147571 : INTERFERON-INDUCED PROTEIN IFI-15K *147572 : INTERFERON-INDUCED PROTEIN IFI-6-16; G1P3 *147573 : INTERFERON PRODUCTION REGULATOR; IFNR *147574 : INTERFERON-STIMULATED TRANSCRIPTION FACTOR 3, GAMMA; ISGF3G *147575 : INTERFERON REGULATORY FACTOR 1; IRF1 *147576 : INTERFERON REGULATORY FACTOR 2; IRF2 *147577 : INTERFERON, ALPHA-10; IFNA10 *147578 : INTERFERON, ALPHA-13; IFNA13 *147579 : INTERFERON, ALPHA-14; IFNA14 *147580 : INTERFERON, ALPHA-16; IFNA16 ^147581 : MOVED TO 100880 *147582 : IRON-RESPONSIVE ELEMENT-BINDING PROTEIN 2; IREB2 *147583 : INTERFERON, ALPHA-17; IFNA17 *147584 : INTERFERON, ALPHA-21; IFNA21 ^147585 : MOVED TO 147660 *147586 : INTERFERON-GAMMA-INDUCIBLE PROTEIN 16; IFI16 147590 : IRIS DYSPLASIA WITH OCULAR HYPERTELORISM, PSYCHOMOTOR RETARDATION AND SENSORINEURAL DEAFNESS 147610 : IRIS PIGMENT LAYER, CLEAVAGE OF *147620 : INTERLEUKIN 6; IL6 *147625 : ISLET CELL AUTOANTIGEN 1; ICA1 147630 : ISLET CELL ADENOMATOSIS *147640 : INTERFERON, BETA-1; IFNB1 *147650 : ISOCITRATE DEHYDROGENASE 2; IDH2 *147660 : INTERFERON, ALPHA-1; IFNA1 *147670 : INSULIN RECEPTOR; INSR *147671 : INSULIN RECEPTOR-RELATED RECEPTOR; INSRR *147678 : CASPASE 1, APOPTOSIS-RELATED CYSTEINE PROTEASE; CASP1 *147679 : INTERLEUKIN 1 RECEPTOR ANTAGONIST; IL1RN *147680 : INTERLEUKIN 2; IL2 *147681 : INTERLEUKIN 11; IL11 *147683 : INTERLEUKIN 13; IL13 *147684 : INTERLEUKIN 14; IL14 *147685 : INTERLEUKIN ENHANCER-BINDING FACTOR 1; ILF1 ^147686 : MOVED TO 300119 *147690 : INTERFERON-INDUCED PROTEIN WITH TETRATRICOPEPTIDE REPEATS 1; IFIT1 *147700 : ISOCITRATE DEHYDROGENASE 1; IDH1 147710 : INTUSSUSCEPTION *147720 : INTERLEUKIN 1-BETA; IL1B *147730 : INTERLEUKIN 2 RECEPTOR, ALPHA; IL2RA *147740 : INTERLEUKIN 3; IL3 *147750 : IVIC SYNDROME *147760 : INTERLEUKIN 1-ALPHA; IL1A 147770 : JOHNSON NEUROECTODERMAL SYNDROME *147780 : INTERLEUKIN 4; IL4 *147781 : INTERLEUKIN 4 RECEPTOR; IL4R *147790 : IMMUNOGLOBULIN J POLYPEPTIDE, LINKER PROTEIN FOR IMMUNOGLOBULIN ALPHA AND MU POLYPEPTIDES; IGJ #147791 : JACOBSEN SYNDROME; JBS *147795 : JANUS KINASE 1; JAK1 *147796 : JANUS KINASE 2; JAK2 *147800 : AASE-SMITH SYNDROME *147810 : INTERLEUKIN 1 RECEPTOR, TYPE I; IL1R1 *147811 : INTERLEUKIN 1 RECEPTOR, TYPE II; IL1R2 147820 : INTERNAL CAROTID ARTERY, SPONTANEOUS DISSECTION OF *147830 : INVASION AND METASTASIS FACTORS ON CHROMOSOME 7; INM7 *147840 : INTERCELLULAR ADHESION MOLECULE 1; ICAM1 *147850 : INTERLEUKIN 5; IL5 *147851 : INTERLEUKIN 5 RECEPTOR, ALPHA; IL5RA *147860 : INTERFERON, BETA-3; IFNB3 *147870 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 2; WNT2 *147880 : INTERLEUKIN 6 RECEPTOR; IL6R *147890 : MYXOVIRUS RESISTANCE 2, MOUSE, HOMOLOG OF; MX2 *147891 : ISCHIOPATELLAR DYSPLASIA *147892 : DEIODINASE, IODOTHYRONINE, TYPE I; DIO1 *147900 : JOINT LAXITY, FAMILIAL *147910 : KALLIKREIN 1; KLK1 147920 : KABUKI SYNDROME *147935 : PROTEASE INHIBITOR 4; PI4 *147940 : ISLET AMYLOID POLYPEPTIDE; IAPP *147950 : KALLMANN SYNDROME 2; KAL2 *147960 : KALLIKREIN 2; KLK2 #148000 : KAPOSI SARCOMA *148020 : KERATIN 19; KRT19 *148021 : KERATIN, CUTICLE, ULTRAHIGH-SULFUR, 1; KRN1 *148022 : KERATIN, CUTICLE, ULTRAHIGH-SULFUR, 1-LIKE; KRN1L *148030 : KERATIN 15; KRT15 *148040 : KERATIN 5; KRT5 *148041 : KERATIN 6A; KRT6A *148042 : KERATIN 6B; KRT6B *148043 : KERATIN 3; KRT3 *148050 : KBG SYNDROME *148059 : KERATIN 7; KRT7 *148060 : KERATIN 8; KRT8 *148065 : KERATIN 13; KRT13 *148066 : KERATIN 14; KRT14 *148067 : KERATIN 16; KRT16 *148069 : KERATIN 17; KRT17 *148070 : KERATIN 18; KRT18 *148080 : KERATIN 10; KRT10 148100 : KELOIDS *148180 : FIBROBLAST GROWTH FACTOR 7; FGF7 ^148181 : MOVED TO 176943 #148190 : KERATITIS, HEREDITARY *148200 : KERATITIS FUGAX HEREDITARIA #148210 : KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT *148300 : KERATOCONUS #148350 : KERATODERMA, PALMOPLANTAR, WITH DEAFNESS 148360 : KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORY NEUROPATHY *148370 : KERATOLYTIC WINTER ERYTHEMA 148390 : KERATOSES, FAMILIAL ACTINIC *148500 : TYLOSIS WITH ESOPHAGEAL CANCER; TOC 148520 : KERATOSIS PALMARIS ET PLANTARIS WITH CLINODACTYLY *148600 : KERATOSIS PALMOPLANTARIS PAPULOSA #148700 : KERATOSIS PALMOPLANTARIS STRIATA I *148730 : KERATOSIS, FOCAL PALMOPLANTAR AND GINGIVAL *148750 : KINASE-LIKE PROTEIN G7P1; G7P1 *148760 : KINESIN-LIKE 1; KNSL1 148800 : KLEEBLATTSCHAEDEL SYNDROME #148820 : KLEIN-WAARDENBURG SYNDROME 148840 : KLEINE-LEVIN HIBERNATION SYNDROME 148860 : KLIPPEL-FEIL DEFORMITY, CONDUCTIVE DEAFNESS, AND ABSENT VAGINA 148870 : KLIPPEL-FEIL DEFORMITY, DEAFNESS, AND FACIAL ASYMMETRY *148900 : KLIPPEL-FEIL SYNDROME 149000 : KLIPPEL-TRENAUNAY-WEBER SYNDROME 149100 : KNUCKLE PADS *149200 : KNUCKLE PADS, LEUKONYCHIA, AND SENSORINEURAL DEAFNESS *149300 : KOILONYCHIA, HEREDITARY #149400 : KOK DISEASE 149500 : KYRLE DISEASE 149600 : LABIA MINORA, INCOMPLETE ADHESION OF 149700 : LACRIMAL DUCT DEFECT *149730 : LACRIMOAURICULODENTODIGITAL SYNDROME; LADD *149750 : LACTALBUMIN, ALPHA; LALBA *150000 : LACTATE DEHYDROGENASE-A; LDHA *150100 : LACTATE DEHYDROGENASE-B; LDHB *150150 : LACTATE DEHYDROGENASE-C; LDHC 150160 : LACTATE DEHYDROGENASE-K; LDHK 150170 : LACTIC ACIDOSIS, CHRONIC ADULT FORM *150200 : CHORIONIC SOMATOMAMMOTROPIN HORMONE 1; CSH1 *150205 : LACTOPEROXIDASE; LPO *150210 : LACTOTRANSFERRIN; LTF 150220 : LACTOSE INTOLERANCE, CONGENITAL #150230 : LANGER-GIEDION SYNDROME; LGS *150240 : LAMININ, BETA-1; LAMB1 *150250 : LARSEN SYNDROME, AUTOSOMAL DOMINANT; LRS1 *150260 : LARYNGEAL ABDUCTOR PARALYSIS *150270 : LARYNGEAL ADDUCTOR PARALYSIS; LAP 150280 : LARYNGOMALACIA *150290 : LAMININ, GAMMA-1; LAMC1 *150292 : LAMININ, GAMMA-2; LAMC2 150300 : LARYNX, CONGENITAL PARTIAL ATRESIA OF *150310 : LAMININ, BETA-3; LAMB3 *150320 : LAMININ, ALPHA-1; LAMA1 *150325 : LAMININ, BETA-2; LAMB2 *150330 : LAMIN A/C; LMNA *150340 : LAMIN B1; LMNB1 *150341 : LAMIN B2; LMNB2 150360 : LARYNGEAL WEB, FAMILIAL *150370 : LAMININ RECEPTOR 1; LAMR1 *150390 : LATENT TRANSFORMING GROWTH FACTOR-BETA-BINDING PROTEIN 1; LTBP1 *150400 : LATERAL INCISORS, ABSENCE OF 150500 : LATTICE DEGENERATION OF RETINA LEADING TO RETINAL DETACHMENT 150550 : LAZY LEUKOCYTE SYNDROME *150570 : LECTIN, BETA-GALACTOSIDE BINDING, SOLUBLE, 1; LGALS1 *150571 : LECTIN, GALACTOSIDE-BINDING, SOLUBLE, 2; LGALS2 150590 : LEG ULCERS, FAMILIAL, OF JUVENILE ONSET 150600 : LEGG-CALVE-PERTHES DISEASE #150699 : LEIOMYOMA, UTERINE 150700 : LEIOMYOMA OF VULVA AND ESOPHAGUS #150800 : LEIOMYOMA, HEREDITARY MULTIPLE, OF SKIN 150900 : LENTIGINES 151000 : LENTIGINOSIS, CENTROFACIAL NEURODYSRAPHIC 151001 : LENTIGINOSIS, INHERITED PATTERNED *151020 : LENTIL AGGLUTININ BINDING 151050 : LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM *151100 : LEOPARD SYNDROME *151200 : LERI PLEONOSTEOSIS #151210 : THANATOPHORIC DYSPLASIA VARIANTS *151250 : LETHAL ANTIGEN--A1; AL-A1 *151290 : CD57 ANTIGEN; CD57 *151300 : LEUCYL-CYSTINYL AMINOPEPTIDASE; LNPEP *151310 : LEUCINE TRANSPORT, HIGH; LEUT *151350 : LEUCYL-tRNA SYNTHETASE; LARS 151380 : LEUKEMIA, ACUTE MONOCYTIC *151385 : RUNT-RELATED TRANSCRIPTION FACTOR 1; RUNX1 *151390 : LEUKEMIA, ACUTE T-CELL; ATL #151400 : LEUKEMIA, CHRONIC LYMPHATIC; CLL *151410 : BREAKPOINT CLUSTER REGION; BCR *151430 : B-CELL CLL/LYMPHOMA 2; BCL2 *151440 : LEUKEMIA, LYMPHOID, 1; LYL1 *151441 : LEUKEMIA/LYMPHOMA, CHRONIC B-CELL, 5; BCL5 *151442 : STATHMIN 1; STMN1 *151443 : LEUKEMIA INHIBITORY FACTOR RECEPTOR; LIFR *151445 : LEUKOCYTE ANTIGEN CD23; CD23 *151450 : LEUKOCYTE ANTIGEN GROUP FIVE; LAG5 *151460 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, C; PTPRC ^151465 : MOVED TO 162643 151500 : LEUKOCYTE NUCLEAR APPENDAGES, HEREDITARY PREVALENCE OF *151510 : INTEGRIN, ALPHA-X; ITGAX *151520 : LEUKOCYTE TYROSINE KINASE; LTK *151523 : LEUKOCYTE SURFACE ANTIGEN CD37; CD37 *151525 : LEUKOCYTE SURFACE ANTIGEN CD53; CD53 *151530 : ALANYL AMINOPEPTIDASE; ANPEP ^151540 : MOVED TO 600623 151550 : LEUKONYCHIA MACULATA *151570 : LEUKOTRIENE A4 HYDROLASE; LTA4H ^151580 : MOVED TO 142360 151590 : LICHEN SCLEROSUS ET ATROPHICUS; LSA *151600 : LEUKONYCHIA TOTALIS 151610 : LEVATOR-MEDIAL RECTUS SYNKINESIS 151620 : LICHEN PLANUS, FAMILIAL #151623 : LI-FRAUMENI SYNDROME; LFS *151625 : LIGATIN *151626 : LINE RETROTRANSPOSABLE ELEMENT 1; LRE1 *151627 : LINKIN *151628 : LINE RETROTRANSPOSABLE ELEMENT 2; LRE2 *151630 : LIP, MEDIAN NODULE OF UPPER 151640 : LIP, HAMARTOMATOUS #151660 : LIPODYSTROPHY, FAMILIAL PARTIAL; FPLD *151670 : LIPASE, HEPATIC; LIPC *151675 : LIPOCALIN 1; LCN1 151680 : LIPODYSTROPHY, PARTIAL, WITH RIEGER ANOMALY, SHORT STATURE, AND INSULINOPENIC DIABETES MELLITUS *151690 : ANNEXIN A1; ANXA1 151700 : LIPOMA OF THE CONJUNCTIVA ^151710 : MOVED TO 151740 ^151720 : MOVED TO 151740 ^151730 : MOVED TO 151740 *151740 : ANNEXIN A2; ANXA2 *151750 : LIPASE, HORMONE-SENSITIVE; LIPE 151800 : LIPOMATOSIS, FAMILIAL BENIGN CERVICAL *151900 : LIPOMATOSIS, MULTIPLE *151990 : LIPOPOLYSACCHARIDE-BINDING PROTEIN; LBP *152100 : LIPOPROTEIN TYPES--Ld SYSTEM *152200 : APOLIPOPROTEIN(a); LPA 152300 : LIPOPROTEIN TYPES--Lt SYSTEM *152310 : TISSUE FACTOR PATHWAY INHIBITOR; TFPI *152390 : ARACHIDONATE 5-LIPOXYGENASE; ALOX5 *152391 : ARACHIDONATE 12-OXIDOREDUCTASE; ALOX12 *152392 : ARACHIDONATE 15-LIPOXYGENASE; ALOX15 152400 : LIPOPROTEIN, VARIANT OF BETA 152420 : LITHIUM TRANSPORT *152422 : LOCUS CONTROL REGION, ALPHA 152423 : LIVER CELL ADHESION MOLECULE; LCAM *152424 : LOCUS CONTROL REGION, BETA *152425 : FATTY ACID CoA LIGASE, LONG-CHAIN 1; FACL1 *152426 : FATTY ACID CoA LIGASE, LONG-CHAIN 2; FACL2 *152427 : LONG QT SYNDROME 2; LQT2 #152430 : LONGEVITY *152445 : LORICRIN; LOR 152450 : LOW DENSITY LIPOPROTEIN, VARIATION IN MOLECULAR WEIGHT *152460 : LOBULAR GLOMERULOPATHY, FAMILIAL 152550 : LUMBAR STENOSIS, FAMILIAL 152600 : LUNULAE OF FINGERNAILS *152690 : THYROID AUTOANTIGEN, 70-KD; G22P1 #152700 : LUPUS ERYTHEMATOSUS, SYSTEMIC; SLE *152760 : GONADOTROPIN-RELEASING HORMONE 1; GNRH1 ^152761 : MOVED TO 138850 *152780 : LUTEINIZING HORMONE, BETA POLYPEPTIDE; LHB *152790 : LUTEINIZING HORMONE/CHORIOGONADOTROPIN RECEPTOR; LHCGR *152800 : LYMPHANGIECTASIA, INTESTINAL 152900 : LYMPHEDEMA AND CEREBRAL ARTERIOVENOUS ANOMALY *152950 : LYMPHEDEMA, MICROCEPHALY, CHORIORETINOPATHY SYNDROME #153000 : LYMPHEDEMA AND PTOSIS #153100 : LYMPHEDEMA, HEREDITARY I *153200 : LYMPHEDEMA, HEREDITARY II *153240 : SELECTIN L; SELL *153243 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 8; TNFRSF8 *153245 : LYMPHOID ENHANCER-BINDING FACTOR 1; LEF1 *153280 : LYMPHOCYTE CYTOSOL POLYPEPTIDE, 40-KD *153290 : LYMPHOCYTE CYTOSOL POLYPEPTIDE, 49-KD 153300 : YELLOW NAIL SYNDROME *153310 : CHARCOT-LEYDEN CRYSTAL PROTEIN; CLC *153330 : LYSOSOME-ASSOCIATED MEMBRANE PROTEIN 1; LAMP1 ^153335 : MOVED TO 182284 *153337 : LYMPHOCYTE ACTIVATION GENE 3; LAG3 *153340 : LYMPHOCYTE ANTIGEN CD5; CD5 ^153360 : MOVED TO 300257 *153370 : INTEGRIN, ALPHA-L; ITGAL *153380 : LYMPHOCYTE CYTOSOL POLYPEPTIDE, 20-KD *153390 : LYMPHOCYTE-SPECIFIC PROTEIN-TYROSINE KINASE; LCK #153400 : LYMPHEDEMA-DISTICHIASIS SYNDROME *153420 : LYMPHOCYTE FUNCTION-ASSOCIATED ANTIGEN, TYPE 3; LFA3 *153430 : LYMPHOCYTE CYTOSOLIC PROTEIN 1; LCP1 *153432 : LYMPHOCYTE-SPECIFIC PROTEIN; LSP1 *153435 : LYMPHOKINE-ACTIVATED KILLER CELL LIGAND; LAKL *153440 : LYMPHOTOXIN-ALPHA; LTA *153450 : LYSOZYME; LYZ *153454 : PROCOLLAGEN-LYSINE, 2-OXOGLUTARATE 5-DIOXYGENASE; PLOD *153455 : LYSYL OXIDASE; LOX *153456 : LYSYL OXIDASE-LIKE 1; LOXL1 153460 : MCARDLE SYNDROME, AUTOSOMAL DOMINANT 153470 : MACROCEPHALY, BENIGN FAMILIAL #153480 : MACROCEPHALY, MULTIPLE LIPOMAS, AND HEMANGIOMATA #153550 : 5q- SYNDROME 153600 : MACROGLOBULINEMIA, WALDENSTROM; WM *153615 : CAPPING PROTEIN, GELSOLIN-LIKE; CAPG *153618 : MACROPHAGE MANNOSE RECEPTOR; MRC1 *153619 : LECTIN, GALACTOSIDE-BINDING, SOLUBLE, 3; LGALS3 *153620 : MACROPHAGE MIGRATION INHIBITORY FACTOR; MIF *153622 : MACROPHAGE SCAVENGER RECEPTOR; MSR1 *153630 : MACROGLOSSIA *153634 : MACROPHAGE ANTIGEN CD68; CD68 #153640 : FECHTNER SYNDROME; FTNS #153650 : EPSTEIN SYNDROME 153670 : MACROTHROMBOCYTOPENIA, BENIGN MEDITERRANEAN *153700 : MACULAR DYSTROPHY, VITELLIFORM; VMD2 #153800 : MACULAR DEGENERATION, AGE-RELATED, 2; ARMD2 *153840 : MACULAR DYSTROPHY, ATYPICAL VITELLIFORM; VMD1 ^153860 : MOVED TO 169150 153870 : MACULAR DYSTROPHY, CONCENTRIC ANNULAR *153880 : MACULAR EDEMA, CYSTOID 153890 : MACULAR DYSTROPHY, FENESTRATED SHEEN TYPE ^153900 : MOVED TO 600110 154000 : MACULES, HEREDITARY CONGENITAL HYPOPIGMENTED AND HYPERPIGMENTED #154020 : HYPOMAGNESEMIA 2, RENAL; HOMG2 *154030 : NUCLEASE-SENSITIVE ELEMENT-BINDING PROTEIN 1; NSEP1 *154040 : MAJOR HISTOCOMPATIBILITY COMPLEX GENE RD *154045 : LENS INTRINSIC MEMBRANE PROTEIN 2, 19-KD; LIM2 *154050 : MAJOR INTRINSIC PROTEIN OF LENS FIBER; MIP *154100 : MALATE DEHYDROGENASE, MITOCHONDRIAL; MDH2 *154200 : MALATE DEHYDROGENASE, SOLUBLE; MDH1 *154230 : SEX REVERSAL, AUTOSOMAL, 2; SRA2 *154235 : MALE GERM CELL-ASSOCIATED KINASE; MAK *154250 : MALIC ENZYME 1; ME1 *154270 : MALIC ENZYME 2; ME2 *154275 : MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 2; MHS2 *154276 : MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 3 *154280 : SUPPRESSOR OF ANCHORAGE INDEPENDENCE 1; SAI1 154300 : MALOCCLUSION DUE TO PROTUBERANT UPPER FRONT TEETH *154360 : MALTASE-GLUCOAMYLASE; MGAM *154365 : PROTEASOME 26S SUBUNIT, ATPase, 2; PSMC2 154370 : MAMMASTATIN 154400 : ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1 #154500 : TREACHER COLLINS-FRANCESCHETTI SYNDROME; TCOF *154540 : MANNOSE 6-PHOSPHATE RECEPTOR, CATION-DEPENDENT; M6PR *154545 : LECTIN, MANNOSE-BINDING, SOLUBLE, 2; MBL2 *154550 : MANNOSEPHOSPHATE ISOMERASE; MPI *154570 : MANNOSE 6-PHOSPHATE RECEPTOR RECOGNITION DEFECT, LEBANESE TYPE *154580 : MANNOSIDASE, ALPHA, CLASS 2C, MEMBER 1; MAN2C1 *154582 : MANNOSIDASE, ALPHA, CLASS 2A, MEMBER 1; MAN2A1 154600 : MARCUS GUNN PHENOMENON #154700 : MARFAN SYNDROME; MFS *154705 : MARFAN-LIKE CONNECTIVE TISSUE DISORDER 154750 : MARFANOID HYPERMOBILITY SYNDROME #154780 : MARSHALL SYNDROME *154790 : PROTEASE INHIBITOR 5; PI5 154800 : MAST CELL DISEASE 154850 : MASTICATORY MUSCLES, HYPERTROPHY OF *154870 : GAMMA-CARBOXYGLUTAMIC ACID PROTEIN, MATRIX; MGP *154950 : MAX PROTEIN; MAX *155000 : MAXILLOFACIAL DYSOSTOSIS *155050 : MAXILLONASAL DYSPLASIA, BINDER TYPE #155100 : MAY-HEGGLIN ANOMALY; MHA *155120 : A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 11; ADAM11 155140 : MECKEL DIVERTICULUM 155145 : CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA 155150 : MEDIAN-ULNAR NERVE COMMUNICATIONS 155200 : MEDIOSTERNAL DEPIGMENTATION LINE #155240 : MEDULLARY THYROID CARCINOMA, FAMILIAL; MTC ^155250 : MOVED TO 130130 #155255 : MEDULLOBLASTOMA *155310 : MEGADUODENUM AND/OR MEGACYSTIS *155350 : MEGALENCEPHALY 155500 : MEGALODACTYLY *155540 : MELANOCORTIN 3 RECEPTOR; MC3R *155541 : MELANOCORTIN 4 RECEPTOR; MC4R *155550 : SILVER, MOUSE, HOMOLOG OF; SILV *155555 : MELANOCORTIN 1 RECEPTOR; MC1R *155600 : MELANOMA, CUTANEOUS MALIGNANT; CMM #155601 : MELANOMA, CUTANEOUS MALIGNANT, 2; CMM2 155700 : MELANOMA, MALIGNANT INTRAOCULAR #155720 : MELANOMA, UVEAL *155730 : GRO1 ONCOGENE; GRO1 *155735 : MELANOMA ADHESION MOLECULE; MCAM *155740 : CD63 ANTIGEN; CD63 ^155741 : MOVED TO 600186 *155750 : MELANOMA-ASSOCIATED ANTIGEN p97; MFI2 #155755 : MELANOMA-ASTROCYTOMA SYNDROME *155760 : AGGRECAN 1; AGC1 155770 : MELANOMA TUMOR ANTIGEN GP90 *155800 : MELANOSIS, UNIVERSAL *155900 : MELKERSSON-ROSENTHAL SYNDROME 155950 : MELORHEOSTOSIS *155960 : MEMBRANE COMPONENT, CHROMOSOME 6, POLYPEPTIDE 2; M6P2 *155970 : MEMBRANE GLYCOPROTEIN MRC OX-2; MOX2 *155975 : MEMBRANE-BOUND IMMUNOGLOBULIN IgM-ALPHA; MB1 *155980 : MEMBRANOUS CRANIAL OSSIFICATION, DELAYED #156000 : MENIERE DISEASE *156100 : MENINGIOMA 1; MN1 156190 : MENTAL AND GROWTH RETARDATION WITH AMBLYOPIA 156200 : MENTAL RETARDATION, DOMINANT 156220 : MERALGIA PARAESTHETICA, FAMILIAL *156225 : LAMININ, ALPHA-2; LAMA2 *156230 : MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE *156232 : MESOMELIC DYSPLASIA, KANTAPUTRA TYPE *156240 : MESOTHELIOMA, MALIGNANT 156250 : METACHONDROMATOSIS 156300 : METACHROMASIA OF FIBROBLASTS 156310 : METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASE A ^156340 : MOVED TO 156360 *156349 : METALLOTHIONEIN 1B; MT1B *156350 : METALLOTHIONEIN 1A; MT1A *156351 : METALLOTHIONEIN 1E; MT1E *156352 : METALLOTHIONEIN 1F; MT1F *156353 : METALLOTHIONEIN 1G; MT1G *156354 : METALLOTHIONEIN 1H; MT1H *156355 : METALLOTHIONEIN 1I; MT1I *156356 : METALLOTHIONEIN 1J; MT1J *156357 : METALLOTHIONEIN 1K; MT1K *156358 : METALLOTHIONEIN 1L; MT1L *156359 : METALLOTHIONEIN 1X; MT1X *156360 : METALLOTHIONEIN 2A; MT2A #156400 : METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE *156490 : NONMETASTATIC CELLS 1, PROTEIN EXPRESSED IN; NME1 *156491 : NONMETASTATIC CELLS 2, PROTEIN EXPRESSED IN; NME2 #156500 : METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS 156510 : METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY *156520 : METATARSUS VARUS, TYPE I 156530 : METATROPIC DYSPLASIA, NONLETHAL DOMINANT *156535 : METHYL-CpG-BINDING DOMAIN PROTEIN 1; MBD1 ^156536 : MOVED TO 600113 *156540 : METHYLTHIOADENOSINE PHOSPHORYLASE; MTAP #156550 : KNIEST DYSPLASIA *156560 : METHIONINE-tRNA SYNTHETASE; MARS *156565 : N-@METHYLPURINE DNA GLYCOSYLASE; MPG *156569 : METHYLGUANINE-DNA METHYLTRANSFERASE; MGMT *156570 : 5-@METHYLTETRAHYDROFOLATE-HOMOCYSTEINE S-METHYLTRANSFERASE; MTR #156575 : MEVALONATE UPTAKE FACILITATOR; MEV *156580 : MICROCEPHALY, AUTOSOMAL DOMINANT 156590 : MICROCEPHALY WITH CHORIORETINOPATHY *156600 : MICROCORIA, CONGENITAL *156610 : MICHELIN TIRE BABY SYNDROME 156620 : MICROCEPHALY-DEAFNESS SYNDROME 156700 : MICROCORNEA, GLAUCOMA, AND ABSENT FRONTAL SINUSES *156790 : MICROFIBRIL-ASSOCIATED PROTEIN 2; MFAP2 #156810 : MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD 156830 : MICROMELIC BONE DYSPLASIA WITH CLOVERLEAF SKULL *156845 : MICROPHTHALMIA-ASSOCIATED TRANSCRIPTION FACTOR; MITF *156850 : MICROPHTHALMIA-CATARACT 156900 : MICROPHTHALMOS WITH MYOPIA AND CORECTOPIA 157100 : MICROPHTHALMOS, PIGMENTARY RETINOPATHY, AND GLAUCOMA *157129 : MICROTUBULE-ASSOCIATED PROTEIN 1B; MAP1B *157130 : MICROTUBULE-ASSOCIATED PROTEIN 2; MAP2 *157132 : MICROTUBULE-ASSOCIATED PROTEIN 4; MAP4 *157140 : MICROTUBULE-ASSOCIATED PROTEIN TAU; MAPT *157145 : MICROSEMINOPROTEIN, BETA; MSMB *157147 : MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN, 88-KD; MTP 157150 : MICROSPHEROPHAKIA WITH HERNIA 157151 : MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA 157160 : MICROTUBULE-ASSOCIATED PROTEIN TAU-LIKE; MAPTL #157170 : HOLOPROSENCEPHALY 2; HPE2 *157200 : MIDPHALANGEAL HAIR *157300 : MIGRAINE WITH AURA, SUSCEPTIBILITY TO; MGAU *157400 : MILIA, MULTIPLE ERUPTIVE ^157500 : MOVED TO 173310 157550 : MINICORE MYOPATHY, DOMINANT *157560 : MINISATELLITE 33.6 *157570 : MINISATELLITE 33.15 157600 : MIRROR MOVEMENTS, HEREDITARY #157640 : PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS; PEO 157650 : MITOCHONDRIAL MYOPATHY, LIPID TYPE *157655 : NADH-UBIQUINONE OXIDOREDUCTASE Fe-S PROTEIN 1; NDUFS1 *157660 : MITOCHONDRIAL RNA-PROCESSING ENDORIBONUCLEASE, RNA COMPONENT OF; RMRP *157670 : TRANSCRIPTION FACTOR 6-LIKE 1; TCF6L1 *157680 : CELL DIVISION CYCLE 25C; CDC25C *157700 : MITRAL VALVE PROLAPSE, FAMILIAL; MVP 157800 : MITRAL REGURGITATION, CONDUCTIVE DEAFNESS, AND FUSION OF CERVICAL VERTEBRAE AND OF CARPAL AND TARSAL BONES 157860 : MIXED LYMPHOCYTE CULTURE LOCUS II *157900 : MOEBIUS SYNDROME 1; MBS1 157910 : MOEBIUS SYNDROME WITH CLUBFOOT, ARTHROGRYPOSIS, AND DIGITAL ANOMALIES ^157920 : MOVED TO 309845 *157950 : MOLAR I REINCLUSION 157960 : MOLONEY LEUKEMIA VIRUS INTEGRATION SITE 2, MOUSE, HOMOLOG OF; MLVI2 *157970 : PROTEASOME 26S SUBUNIT, NON-ATPase, 7; PSMD7 ^157975 : MOVED TO 172411 157980 : MOMO SYNDROME #158000 : MONILETHRIX 158020 : ANTIGEN DEFINED BY MONOCLONAL ANTIBODY 4F2, LIGHT CHAIN *158030 : ANTIGEN DEFINED BY MONOCLONAL ANTIBODY AJ9; MSK1 *158040 : ANTIGEN DEFINED BY MONOCLONAL ANTIBODY T87; MSK2 *158050 : MONKEY RED BLOOD CELL RECEPTOR; MRBC *158070 : SOLUTE CARRIER FAMILY 3 (ACTIVATOR OF DIBASIC AND NEUTRAL AMINO ACID TRANSPORT), MEMBER 2; SLC3A2 158100 : MONOPHALANGY OF GREAT TOE *158105 : SMALL INDUCIBLE CYTOKINE A2; SCYA2 *158106 : SMALL INDUCIBLE CYTOKINE A7; SCYA7 *158120 : MONOCYTE DIFFERENTIATION ANTIGEN CD14; CD14 ^158130 : MOVED TO 158105 *158150 : MONOPHOSPHOGLYCERATE MUTASE #158170 : MONOSOMY 9p SYNDROME 158250 : MOSAICISM, CHROMOSOMAL *158270 : MOTILIN; MLN 158280 : MOTION SICKNESS *158300 : MOUTH, INABILITY TO OPEN COMPLETELY, AND SHORT FINGER-FLEXOR TENDONS *158310 : MUCOEPITHELIAL DYSPLASIA, HEREDITARY #158320 : MUIR-TORRE SYNDROME; MTS #158330 : MULLERIAN APLASIA *158340 : MUCIN 1, TRANSMEMBRANE; MUC1 *158343 : ATP-BINDING CASSETTE, SUBFAMILY C, MEMBER 1; ABCC1 158345 : MULTIPLE EXOSTOSES WITH SPASTIC TETRAPARESIS #158350 : COWDEN DISEASE; CD *158370 : MUCIN 2, INTESTINAL; MUC2 *158371 : MUCIN 3A, INTESTINAL; MUC3A *158372 : MUCIN 4, TRACHEOBRONCHIAL; MUC4 *158373 : MUCIN 5, SUBTYPES A AND C, TRACHEOBRONCHIAL; MUC5AC *158374 : MUCIN 6, GASTRIC; MUC6 *158375 : MUCIN 7, SALIVARY; MUC7 *158378 : SOLUTE CARRIER FAMILY 20, MEMBER 2; SLC20A2 *158380 : ECOTROPIC VIRAL INTEGRATION SITE 2A; EVI2A *158381 : ECOTROPIC VIRAL INTEGRATION SITE 2B; EVI2B *158400 : MUSCLE CRAMPS, FAMILIAL *158500 : MUSCULAR ATROPHY, ATAXIA, RETINITIS PIGMENTOSA, AND DIABETES MELLITUS *158580 : MOTOR NEURONOPATHY, DISTAL HEREDITARY, WITH VOCAL CORD PARALYSIS *158590 : MUSCULAR ATROPHY, ADULT SPINAL *158600 : MUSCULAR ATROPHY, JUVENILE SPINAL 158650 : MUSCULAR ATROPHY, MALIGNANT NEUROGENIC #158700 : MUSCULAR ATROPHY, PROGRESSIVE, WITH AMYOTROPHIC LATERAL SCLEROSIS 158800 : MUSCULAR DYSTROPHY, BARNES TYPE #158810 : MYOPATHY, BENIGN CONGENITAL, WITH CONTRACTURES *158900 : FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A *158901 : FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B; FSHMD1B #159000 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1A; LGMD1A #159001 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B; LGMD1B *159050 : MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC, WITH INTERNALIZED CAPILLARIES 159100 : MUSCULAR HYPOPLASIA, CONGENITAL UNIVERSAL, OF KRABBE 159300 : MUSICAL PERFECT PITCH *159350 : MUTATED IN COLORECTAL CANCERS; MCC 159400 : MYASTHENIA, FAMILIAL LIMB-GIRDLE *159405 : V-MYB AVIAN MYELOBLASTOSIS VIRAL ONCOGENE HOMOLOG-LIKE 1; MYBL1 159410 : MYDRIATIC RESPONSE TO PHARMACOLOGIC AGENTS 159420 : MYDRIASIS, CONGENITAL *159430 : MYELIN BASIC PROTEIN; MBP *159440 : MYELIN PROTEIN ZERO; MPZ ^159455 : MOVED TO 170715 *159460 : MYELIN-ASSOCIATED GLYCOPROTEIN; MAG *159465 : MYELIN-OLIGODENDROCYTE GLYCOPROTEIN; MOG 159500 : MYELINATED OPTIC NERVE FIBERS *159530 : MYELOPROLIFERATIVE LEUKEMIA VIRUS ONCOGENE; MPL *159540 : LEUKEMIA-INHIBITORY FACTOR; LIF 159550 : MYELOCEREBELLAR DISORDER *159552 : MYELOID CELL LEUKEMIA 1; MCL1 *159553 : MYELOID CELL NUCLEAR DIFFERENTIATION ANTIGEN; MNDA *159555 : MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA; MLL *159556 : MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 1; MLLT1 *159557 : MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 2; MLLT2 *159558 : MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 3; MLLT3 *159559 : MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 4; MLLT4 159580 : MYELOPATHY, HTLV-1-ASSOCIATED; HAM *159590 : CD33 ANTIGEN; CD33 *159595 : MYELOPROLIFERATIVE SYNDROME, TRANSIENT *159600 : MYOCLONIC EPILEPSY, HARTUNG TYPE 159700 : MYOCLONUS AND ATAXIA 159800 : MYOCLONUS, CEREBELLAR ATAXIA, AND DEAFNESS #159900 : MYOCLONIC DYSTONIA 159950 : MYOCLONUS, HEREDITARY, WITH PROGRESSIVE DISTAL MUSCULAR ATROPHY *159970 : MYOGENIC DIFFERENTIATION ANTIGEN 1; MYOD1 *159980 : MYOGENIC FACTOR 4; MYOG *159990 : MYOGENIC FACTOR 5; MYF5 *159991 : MYOGENIC FACTOR 6; MYF6 *160000 : MYOGLOBIN; MB *160010 : MYOGLOBINURIA, AUTOSOMAL DOMINANT *160100 : MYOKYMIA #160120 : EPISODIC ATAXIA, TYPE 1; EA1 #160150 : MYOPATHY, CENTRONUCLEAR 160200 : MYOPATHY, CONGENITAL, WITH CRYSTALLINE INTRANUCLEAR INCLUSIONS *160300 : MYOPATHY, DISTAL, WITH ONSET IN INFANCY *160500 : MYOPATHY, DISTAL 1; MPD1 160550 : MYOPATHY, MITOCHONDRIAL, WITH CATARACT *160565 : MYOPATHY, TUBULAR AGGREGATE 160570 : MYOPATHY WITH STORAGE OF GLYCOPROTEINS AND GLYCOSAMINOGLYCANS *160700 : MYOPIA 2; MYP2 *160710 : MYOSIN, HEAVY CHAIN 6, CARDIAC MUSCLE, ALPHA; MYH6 *160720 : MYOSIN, HEAVY CHAIN 3, SKELETAL MUSCLE, EMBRYONIC; MYH3 *160730 : MYOSIN, HEAVY CHAIN 1, SKELETAL MUSCLE, ADULT; MYH1 *160740 : MYOSIN, HEAVY CHAIN 2, SKELETAL MUSCLE, ADULT; MYH2 *160741 : MYOSIN, HEAVY CHAIN 8, SKELETAL MUSCLE, PERINATAL; MYH8 *160742 : MYOSIN, HEAVY CHAIN 4, SKELETAL MUSCLE; MYH4 *160745 : MYOSIN, HEAVY CHAIN 11, SMOOTH MUSCLE; MYH11 *160750 : MYOSITIS *160760 : MYOSIN, HEAVY CHAIN 7, CARDIAC MUSCLE, BETA; MYH7 *160770 : MYOSIN, LIGHT CHAIN 4, ALKALI, ATRIAL, EMBRYONIC; MYL4 *160775 : MYOSIN, HEAVY CHAIN 9, NONMUSCLE; MYH9 *160776 : MYOSIN, HEAVY CHAIN 10, NONMUSCLE; MYH10 *160777 : MYOSIN VA; MYO5A *160780 : MYOSIN, LIGHT POLYPEPTIDE 1, ALKALI, SKELETAL, FAST; MYL1 *160781 : MYOSIN, LIGHT CHAIN 2, REGULATORY, CARDIAC, SLOW; MYL2 *160782 : MYOSIN, LIGHT CHAIN 5, REGULATORY; MYL5 *160790 : MYOSIN, LIGHT CHAIN 3, ALKALI, VENTRICULAR, SKELETAL, SLOW; MYL3 *160793 : MYOSIN-BINDING PROTEIN C, FAST TYPE; MYBPC2 *160794 : MYOSIN-BINDING PROTEIN C, SLOW TYPE; MYBPC1 *160795 : MYOSIN-BINDING PROTEIN H; MYBPH #160800 : MYOTONIA CONGENITA, AUTOSOMAL DOMINANT #160900 : DYSTROPHIA MYOTONICA 1 #160980 : CARNEY COMPLEX, TYPE 1; CNC1 160990 : MYOTONIC MYOPATHY WITH CYLINDRICAL SPIRALS *160993 : N-MYRISTOYLTRANSFERASE 1; NMT1 *160994 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M; HNRPM *160995 : ALPHA-1,3-@MANNOSYL-GLYCOPROTEIN BETA-1,2-N-ACETYLGLUCOSAMINYLTRANSFERASE; MGAT1 *160998 : NAD(P)H:MENADIONE OXIDOREDUCTASE 1, DIOXIN-INDUCIBLE 2; NMOR2 *161000 : NAEGELI SYNDROME *161015 : NADH-UBIQUINONE OXIDOREDUCTASE FLAVOPROTEIN 1; NDUFV1 *161050 : NAIL DYSPLASIA 161070 : NAIL HIGH-SULFUR PROTEIN 161080 : NAIL LOW-SULFUR PROTEIN 161100 : NAILBEDS, PIGMENTATION OF #161200 : NAIL-PATELLA SYNDROME; NPS #161400 : NARCOLEPSY 161470 : NASAL ALAR COLLAPSE, BILATERAL 161480 : NASAL BONES, ABSENCE OF *161500 : NASAL GROOVE, FAMILIAL TRANSVERSE 161530 : NASAL HYPERPIGMENTATION, FAMILIAL TRANSVERSE #161550 : NASOPHARYNGEAL CARCINOMA *161555 : KILLER CELL LECTIN-LIKE RECEPTOR, SUBFAMILY C, MEMBER 1; KLRC1 *161560 : INTERLEUKIN 12A; IL12A *161561 : INTERLEUKIN 12B; IL12B *161565 : NATURAL KILLER TUMOR RECOGNITION SEQUENCE; NKTR 161600 : NAVICULAR BONE, ACCESSORY *161650 : NEBULIN; NEB 161700 : NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT #161800 : NEMALINE MYOPATHY 1, AUTOSOMAL DOMINANT; NEM1 *161900 : RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION *161950 : IgA NEPHROPATHY *162000 : NEPHROPATHY, FAMILIAL, WITH GOUT *162010 : NERVE GROWTH FACTOR RECEPTOR; NGFR 162020 : NERVE GROWTH FACTOR, ALPHA SUBUNIT; NGFA *162030 : NERVE GROWTH FACTOR, BETA SUBUNIT; NGFB *162040 : NERVE GROWTH FACTOR, GAMMA SUBUNIT; NGFG *162060 : GROWTH ASSOCIATED PROTEIN 43; GAP43 *162080 : NEURAL RETINA LEUCINE ZIPPER; NRL 162091 : SCHWANNOMATOSIS *162095 : PLEIOTROPHIN; PTN *162096 : NEURITE GROWTH-PROMOTING FACTOR 2; NEGF2 *162100 : NEURITIS WITH BRACHIAL PREDILECTION; NAPB *162150 : PROPROTEIN CONVERTASE, SUBTILISIN/KEXIN-TYPE, 1; PCSK1 *162151 : PROPROTEIN CONVERTASE, SUBTILISIN/KEXIN-TYPE, 2; PCSK2 *162200 : NEUROFIBROMATOSIS, TYPE I; NF1 #162210 : NEUROFIBROMATOSIS, FAMILIAL SPINAL 162220 : NEUROFIBROMATOSIS, FAMILIAL INTESTINAL; NF3B *162230 : NEUROFILAMENT PROTEIN, HEAVY POLYPEPTIDE; NEFH 162240 : NEUROFIBROMATOSIS-PHEOCHROMOCYTOMA-DUODENAL CARCINOID SYNDROME *162250 : NEUROFILAMENT 3; NEF3 162260 : NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL; NF3A 162270 : NEUROFIBROMATOSIS, TYPE IV, OF RICCARDI; NF4 *162280 : NEUROFILAMENT PROTEIN, LIGHT POLYPEPTIDE; NEFL #162300 : MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB; MEN2B *162320 : TACHYKININ 1; TAC1 *162321 : TACHYKININ RECEPTOR 2; TACR2 *162323 : TACHYKININ RECEPTOR 1; TACR1 *162330 : TACHYKININ 3; TAC3 *162332 : TACHYKININ RECEPTOR 3; TACR3 *162340 : NEUROMEDIN B; NMB *162341 : NEUROMEDIN B RECEPTOR; NMBR *162350 : CEROID LIPOFUSCINOSIS, NEURONAL, DOMINANT OR PARRY TYPE *162360 : NESCIENT HELIX LOOP HELIX 1; NHLH1 *162361 : NESCIENT HELIX LOOP HELIX 2; NHLH2 *162370 : NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX *162375 : NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH EXCESSIVE MYELIN FOLDING COMPLEX, AUTOSOMAL DOMINANT 162380 : NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE #162400 : NEUROPATHY, HEREDITARY SENSORY, TYPE I; HSN1 #162500 : NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP 162600 : NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE *162640 : NEUROPEPTIDE Y; NPY *162641 : NEUROPEPTIDE Y RECEPTOR Y1; NPY1R *162642 : NEUROPEPTIDE Y RECEPTOR Y2; NPY2R *162643 : CHEMOKINE (C-X-C) RECEPTOR 4; CXCR4 *162650 : NEUROTENSIN; NTS *162651 : NEUROTENSIN RECEPTOR 1; NTSR1 *162660 : NEUROTROPHIN 3; NTF3 ^162661 : MOVED TO 162662 *162662 : NEUROTROPHIN 5; NTF5 *162700 : NEUTROPENIA, CHRONIC FAMILIAL #162800 : CYCLIC HEMATOPOIESIS *162815 : NEUTROPHIL AZUROCIDIN; NAZC *162820 : NEUTROPHIL CHEMOTACTIC RESPONSE; NCR 162830 : NEUTROPHILIA, HEREDITARY *162860 : NEUTROPHIL-SPECIFIC ANTIGEN: NB ^162870 : MOVED TO 146740 *162880 : NEUTROPHIL-SPECIFIC ANTIGEN: ND1 *162890 : NEUTROPHIL-SPECIFIC ANTIGEN: NE1 *162900 : NEVI *163000 : NEVI FLAMMEI, FAMILIAL MULTIPLE 163050 : NEVUS ANEMICUS *163100 : NEVUS FLAMMEUS OF NAPE OF NECK 163200 : NEVUS SEBACEUS OF JADASSOHN *163260 : NUCLEAR FACTOR ERYTHROID 2-LIKE 1; NFE2L1 *163400 : NIEVERGELT SYNDROME #163500 : NIGHT BLINDNESS, CONGENITAL STATIONARY; CSNB3 163600 : NIPPLES INVERTED *163700 : NIPPLES, SUPERNUMERARY *163728 : NITRIC OXIDE SYNTHASE, CHONDROCYTE *163729 : NITRIC OXIDE SYNTHASE 3; NOS3 *163730 : NITRIC OXIDE SYNTHASE 2A; NOS2A *163731 : NITRIC OXIDE SYNTHASE 1; NOS1 *163800 : NODAL RHYTHM 163850 : NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES *163890 : SYNUCLEIN, ALPHA; SNCA ^163900 : REMOVED FROM DATABASE *163905 : HIGH MOBILITY GROUP PROTEIN 1; HMG1 *163906 : HIGH MOBILITY GROUP PROTEIN 2; HMG2 *163910 : HIGH MOBILITY GROUP PROTEIN 17; HMG17 *163920 : HIGH MOBILITY GROUP PROTEIN 14; HMG14 #163950 : NOONAN SYNDROME 1; NS1 #163955 : NOONAN-LIKE/MULTIPLE GIANT CELL LESION SYNDROME *163970 : SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, NORADRENALINE), MEMBER 2; SLC6A2 *163980 : CARCINOEMBRYONIC ANTIGEN-RELATED CELL ADHESION MOLECULE 6; CEACAM6 164000 : NOSE, ANOMALOUS SHAPE OF *164005 : NUCLEAR FACTOR I/X; NFIX *164008 : NUCLEAR FACTOR OF KAPPA LIGHT CHAIN GENE ENHANCER IN B CELLS INHIBITOR, ALPHA; NFKBIA *164009 : NUCLEAR MITOTIC APPARATUS PROTEIN 1; NUMA1 *164010 : PROCOLLAGEN, TYPE III, N-ENDOPEPTIDASE; PCOLN3 *164011 : NUCLEAR FACTOR KAPPA-B, SUBUNIT 1; NFKB1 *164012 : NUCLEAR FACTOR KAPPA-B, SUBUNIT 2; NFKB2 *164013 : NUCLEAR FACTOR RELATED TO KAPPA-B BINDING PROTEIN; NFRKB *164014 : V-REL AVIAN RETICULOENDOTHELIOSIS VIRAL ONCOGENE HOMOLOG A; RELA *164015 : NUCLEAR MATRIN ^164016 : MOVED TO 600489 *164017 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN A1; HNRPA1 ^164018 : MOVED TO 600124 ^164019 : MOVED TO 600124 *164020 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN C; HNRPC *164021 : NUCLEAR RIBONUCLEOPROTEIN PARTICLE L PROTEIN ^164022 : MOVED TO 300199 *164031 : NUCLEOLAR PROTEIN 1; NOL1 *164035 : NUCLEOLIN; NCL *164040 : NUCLEOPHOSMIN/NUCLEOPLASMIN FAMILY, MEMBER 1; NPM1 *164050 : NUCLEOSIDE PHOSPHORYLASE; NP *164060 : NUCLEOSOME ASSEMBLY PROTEIN 1-LIKE 1; NAP1L1 *164100 : NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT; NYS2 *164150 : NYSTAGMUS, HEREDITARY VERTICAL *164160 : LEPTIN; LEP *164170 : NYSTAGMUS, VOLUNTARY *164175 : POU DOMAIN, CLASS 2, TRANSCRIPTION FACTOR 1; POU2F1 *164176 : POU DOMAIN, CLASS 2, TRANSCRIPTION FACTOR 2; POU2F2 *164177 : POU DOMAIN, CLASS 5, TRANSCRIPTION FACTOR 1; POU5F1 164180 : OCULOCEREBROCUTANEOUS SYNDROME 164185 : OCULAR CICATRICIAL PEMPHIGOID; OCP 164190 : OCULAR DOMINANCE *164200 : OCULODENTODIGITAL DYSPLASIA; ODDD *164210 : HEMIFACIAL MICROSOMIA; HFM 164220 : OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS *164230 : OBSESSIVE-COMPULSIVE DISORDER 1; OCD1 *164280 : OCULODIGITOESOPHAGODUODENAL SYNDROME #164300 : OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD 164310 : OCULOPHARYNGODISTAL MYOPATHY *164320 : ODORANT-BINDING PROTEIN 164330 : ODONTOMA-DYSPHAGIA SYNDROME *164340 : OLFACTORY MARKER PROTEIN; OMP *164342 : OLFACTORY RECEPTOR, FAMILY 1, SUBFAMILY D, MEMBER 2; OR1D2 *164343 : EARLY B-CELL FACTOR; EBF *164345 : OLIGODENDROCYTE-MYELIN GLYCOPROTEIN; OMG *164350 : 2-PRIME,5-PRIME-@OLIGOADENYLATE SYNTHETASE 1; OAS1 *164360 : ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL F1 COMPLEX, ALPHA SUBUNIT, ISOFORM 1; ATP5A1 #164400 : SPINOCEREBELLAR ATAXIA 1; SCA1 *164500 : SPINOCEREBELLAR ATAXIA 7; SCA7 164600 : OLIVOPONTOCEREBELLAR ATROPHY IV 164680 : ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR *164690 : V-ABL ABELSON MURINE LEUKEMIA VIRAL ONCOGENE HOMOLOG 2; ABL2 *164700 : OLIVOPONTOCEREBELLAR ATROPHY V; OPCA V ^164710 : REMOVED FROM DATABASE *164720 : V-ETS AVIAN ERYTHROBLASTOSIS VIRUS E26 ONCOGENE HOMOLOG 1; ETS1 *164730 : V-AKT MURINE THYMOMA VIRAL ONCOGENE HOMOLOG 1; AKT1 *164731 : V-AKT MURINE THYMOMA VIRAL ONCOGENE HOMOLOG 2; AKT2 *164740 : V-ETS AVIAN ERYTHROBLASTOSIS VIRUS E26 ONCOGENE HOMOLOG 2; ETS2 164745 : OMODYSPLASIA 164750 : OMPHALOCELE *164755 : VIRAL INTEGRATION SITE 1; VIS1 *164756 : VIRAL INTEGRATION SITE 2 *164757 : V-RAF MURINE SARCOMA VIRAL ONCOGENE HOMOLOG B1; BRAF *164759 : ONCOGENE OVC *164760 : V-RAF-1 MURINE LEUKEMIA VIRAL ONCOGENE HOMOLOG 1; RAF1 *164761 : RET PROTOONCOGENE; RET *164762 : V-CRK AVIAN SARCOMA VIRUS CT10 ONCOGENE HOMOLOG; CRK *164765 : ONCOGENE EMS1; EMS1 *164770 : COLONY-STIMULATING FACTOR 1 RECEPTOR; CSF1R *164772 : V-FOS FBJ MURINE OSTEOSARCOMA VIRAL ONCOGENE HOMOLOG B; FOSB *164780 : V-SKI AVIAN SARCOMA VIRAL ONCOGENE HOMOLOG; SKI *164785 : MOUSE DOUBLE MINUTE 2 HOMOLOG; MDM2 *164790 : NEUROBLASTOMA RAS VIRAL ONCOGENE HOMOLOG; NRAS *164795 : ONCOMODULIN; OCM 164800 : ONYCHOLYSIS, PARTIAL, WITH SCLERONYCHIA *164810 : V-FOS FBJ MURINE OSTEOSARCOMA VIRAL ONCOGENE HOMOLOG; FOS *164820 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 1; WNT1 ^164830 : REMOVED FROM DATABASE *164831 : LEUKEMIA VIRAL BMI-1 ONCOGENE, MOUSE, HOMOLOG OF; BMI1 *164840 : V-MYC AVIAN MYELOCYTOMATOSIS VIRAL-RELATED ONCOGENE, NEUROBLASTOMA-DERIVED; MYCN *164850 : V-MYC AVIAN MYELOCYTOMATOSIS VIRAL ONCOGENE HOMOLOG 1, LUNG CARCINOMA-DERIVED; MYCL1 *164860 : MET PROTOONCOGENE; MET *164865 : V-MYC AVIAN MYELOCYTOMATOSIS VIRAL ONCOGENE HOMOLOG-LIKE 1; MYCLK1 *164870 : V-ERB-B2 AVIAN ERYTHROBLASTIC LEUKEMIA VIRAL ONCOGENE HOMOLOG 2; ERBB2 *164873 : ETS VARIANT GENE 3; ETV3 *164874 : FORKHEAD BOX G1B; FOXG1B *164875 : VAV1 ONCOGENE; VAV1 *164880 : V-YES-1 YAMAGUCHI SARCOMA VIRAL ONCOGENE; YES1 164891 : ONCOGENE YUASA *164900 : OPHTHALMOMANDIBULOMELIC DYSPLASIA ^164905 : MOVED TO 600326 *164910 : V-REL AVIAN RETICULOENDOTHELIOSIS VIRAL ONCOGENE HOMOLOG; REL *164920 : V-KIT HARDY-ZUCKERMAN 4 FELINE SARCOMA VIRAL ONCOGENE HOMOLOG; KIT *164940 : GARDNER-RASHEED FELINE SARCOMA VIRAL ONCOGENE HOMOLOG; FGR *164950 : FIBROBLAST GROWTH FACTOR 3; FGF3 *164951 : NOTCH, DROSOPHILA, HOMOLOG OF, 4; NOTCH4 *164953 : ONCOGENE LIPOSARCOMA; LPSA *164958 : NEPHROBLASTOMA OVEREXPRESSED GENE; NOV *164960 : ONCOGENE PIM 1; PIM1 #164970 : ONCOGENE TRK *164975 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 5A; WNT5A *164980 : FIBROBLAST GROWTH FACTOR 4; FGF4 *165000 : OPHTHALMOPLEGIA, FAMILIAL STATIC ^165010 : MOVED TO 164710 *165020 : V-ROS AVIAN UR2 SARCOMA VIRUS ONCOGENE HOMOLOG 1; ROS1 *165040 : ONCOGENE MEL; MEL *165060 : TRANSFER RNA PHOSPHOSERINE; TRSP *165070 : FMS-RELATED TYROSINE KINASE 1; FLT1 *165080 : V-ETS AVIAN ERYTHROBLASTOSIS VIRUS E26 ONCOGENE RELATED; ERG *165090 : RELATED RAS VIRAL ONCOGENE HOMOLOG; RRAS *165095 : ONCOSTATIN M; OSM 165098 : OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION *165110 : S13 AVIAN ERYTHROBLASTOSIS ONCOGENE HOMOLOG; SEA *165120 : V-YES-1 YAMAGUCHI SARCOMA VIRAL RELATED ONCOGENE HOMOLOG; LYN *165140 : ONCOGENE PVT-1; PVT1 165150 : OPHTHALMOPLEGIA, PROGRESSIVE, WITH SCROTAL TONGUE AND MENTAL DEFICIENCY *165160 : V-JUN AVIAN SARCOMA VIRUS 17 ONCOGENE HOMOLOG; JUN *165161 : ONCOGENE JUN-B; JUNB *165162 : ONCOGENE JUN-D; JUND *165170 : SPLEEN FOCUS FORMING VIRUS PROVIRAL INTEGRATION ONCOGENE SPI1; SPI1 *165180 : MAS1 ONCOGENE; MAS1 *165190 : FIBROBLAST GROWTH FACTOR 5; FGF5 *165195 : OPIOID RECEPTOR, DELTA-1; OPRD1 *165196 : OPIOID RECEPTOR, KAPPA-1; OPRK1 165199 : OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY 165200 : OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS *165210 : ONCOGENE BMYC; BMYC *165215 : ECOTROPIC VIRAL INTEGRATION SITE 1; EVI1 *165220 : GLIOMA-ASSOCIATED ONCOGENE HOMOLOG; GLI *165230 : GLI-KRUPPEL FAMILY MEMBER 2; GLI2 *165240 : GLI-KRUPPEL FAMILY MEMBER 3; GLI3 *165250 : GLI-KRUPPEL FAMILY MEMBER HKR1; HKR1 *165260 : GLI-KRUPPEL FAMILY MEMBER HKR2; HKR2 *165270 : GLI-KRUPPEL FAMILY MEMBER HKR3; HKR3 *165280 : GLI-KRUPPEL FAMILY MEMBER 4; GLI4 *165290 : ONCOGENE RMYC; RMYC 165300 : OPTIC ATROPHY, CATARACT, AND NEUROLOGIC DISORDER *165320 : LIVER CANCER ONCOGENE; LCO *165330 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 3; WNT3 *165340 : SKI-LIKE; SKIL ^165350 : MOVED TO 311040 *165360 : CAS-BR-M MURINE ECOTROPIC RETROVIRAL TRANSFORMING SEQUENCE HOMOLOG; CBL *165370 : RAS HOMOLOG GENE FAMILY, MEMBER B; ARHB *165380 : RAS HOMOLOG GENE FAMILY, MEMBER C; ARHC *165390 : RAS HOMOLOG GENE FAMILY, MEMBER A; ARHA 165490 : OPTIC ATROPHY, DEAFNESS, OPHTHALMOPLEGIA, AND MYOPATHY #165500 : OPTIC ATROPHY 1; OPA1 165510 : OPTIC ATROPHY WITH NEGATIVE ELECTRORETINOGRAMS 165550 : OPTIC NERVE HYPOPLASIA, FAMILIAL BILATERAL 165590 : ORAL-FACIAL-DIGITAL SYNDROME WITH FIBULAR APLASIA 165600 : ORBITAL MARGIN, HYPOPLASIA OF 165630 : ORGANOID NEVUS PHAKOMATOSIS ^165635 : MOVED TO 258870 *165640 : ORNITHINE DECARBOXYLASE 1; ODC1 ^165650 : MOVED TO 165640 *165660 : OSLAM SYNDROME 165670 : OSSIFIED EAR CARTILAGES 165680 : OSSICULAR MALFORMATIONS, FAMILIAL *165700 : OSTEOARTHROPATHY OF FINGERS, FAMILIAL *165720 : OSTEOARTHRITIS *165800 : OSTEOCHONDRITIS DISSECANS; OD #166000 : ENCHONDROMATOSIS, MULTIPLE #166200 : OSTEOGENESIS IMPERFECTA, TYPE I #166210 : OSTEOGENESIS IMPERFECTA CONGENITA; OIC #166220 : OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 166230 : OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES 166240 : OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH 166250 : OSTEOGLOPHONIC DWARFISM 166260 : OSTEOGENESIS IMPERFECTA WITH UNUSUAL SKELETAL LESIONS *166300 : OSTEOLYSIS, HEREDITARY, OF CARPAL BONES WITH NEPHROPATHY #166350 : OSSEOUS HETEROPLASIA, PROGRESSIVE 166400 : OSTEOMAS OF MANDIBLE 166450 : OSTEOMESOPYKNOSIS *166490 : SECRETED PHOSPHOPROTEIN 1; SPP1 166500 : OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS; OSCS *166600 : OSTEOPETROSIS, AUTOSOMAL DOMINANT, TYPE II *166700 : OSTEOPOIKILOSIS 166705 : OSTEOPOIKILOSIS AND DACRYOCYSTITIS #166710 : OSTEOPOROSIS, INVOLUTIONAL ^166720 : MOVED TO 130720 166740 : OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES *166750 : OTODENTAL DYSPLASIA 166760 : OTITIS MEDIA, SUSCEPTIBILITY TO #166780 : OTOFACIOCERVICAL SYNDROME *166800 : OTOSCLEROSIS; OTSC1 166900 : OVALOCYTOSIS, HEREDITARY HEMOLYTIC 166910 : OVALOCYTOSIS, HEREDITARY HEMOLYTIC, WITH DEFECTIVE ERYTHROPOIESIS *166945 : MEMBRANE COMPONENT, CHROMOSOME 17, SURFACE MARKER 2; M17S2 166950 : OVARIAN TERATOMA 166970 : OVARIAN FIBROMATA 166990 : OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA, HYDROCEPHALUS, AND HYPERTENSION *167000 : SUPPRESSOR OF TUMORIGENICITY 8; ST8 *167030 : OXALATE, INCREASED MEMBRANE TRANSPORT FOR *167040 : OXYSTEROL-BINDING PROTEIN; OSBP *167050 : OXYTOCIN--NEUROPHYSIN I; OXT *167055 : OXYTOCIN RECEPTOR; OXTR 167100 : PACHYDERMOPERIOSTOSIS; PDP #167200 : PACHYONYCHIA CONGENITA, TYPE 1; PC1 #167210 : PACHYONYCHIA CONGENITA, TYPE 2; PC2 167220 : PACMAN DYSPLASIA 167250 : PAGET DISEASE OF BONE 1; PDB1 167300 : PAGET DISEASE, EXTRAMAMMARY 167320 : PAGETOID AMYOTROPHIC LATERAL SCLEROSIS *167400 : PAIN, SUBMANDIBULAR, OCULAR AND RECTAL, WITH FLUSHING *167405 : PAIRED BASIC AMINO ACID CLEAVING ENZYME 4; PACE4 *167409 : PAIRED BOX GENE 2; PAX2 *167410 : PAIRED BOX GENE 7; PAX7 *167411 : PAIRED BOX GENE 1; PAX1 *167413 : PAIRED BOX GENE 4; PAX4 *167414 : PAIRED BOX GENE 5; PAX5 *167415 : PAIRED BOX GENE 8; PAX8 *167416 : PAIRED BOX GENE 9; PAX9 *167420 : PAIRED MESODERM HOMEO BOX 1; PMX1 167500 : PALATOPHARYNGEAL INCOMPETENCE 167600 : PALMARIS LONGUS MUSCLE, ABSENCE OF 167700 : PALMOMENTAL REFLEX *167730 : PALPEBRAL COLOBOMA-LIPOMA SYNDROME 167750 : PANCREAS, ANNULAR 167755 : PANCREAS, DORSAL, AGENESIS OF *167770 : REGENERATING ISLET-DERIVED 1-ALPHA; REG1A *167771 : REGENERATING ISLET-DERIVED, RAT, HOMOLOG-LIKE; REGL *167780 : PANCREATIC POLYPEPTIDE/PANCREATIC ICOSAPEPTIDE; PPY *167790 : SERINE PROTEASE INHIBITOR, KAZAL-TYPE, 1; SPINK1 #167800 : PANCREATITIS, HEREDITARY; PCTT *167805 : PANCREATITIS-ASSOCIATED PROTEIN; PAP 167850 : PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE 167870 : PANIC DISORDER 167900 : PAPILLOMATOSIS, FAMILIAL CUTANEOUS 167950 : PAPILLOMATOSIS, FLORID, OF NIPPLE 167959 : HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 1; HPV18I1 167960 : HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 2; HPV18I2 #168000 : PARAGANGLIOMAS, FAMILIAL NONCHROMAFFIN, 1; PGL1 168100 : PARALYSIS AGITANS, JUVENILE, OF HUNT 168200 : PARAMOLAR TUBERCLE OF BOLK #168300 : PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC 168350 : PARAMYOTONIA WITHOUT COLD PARALYSIS *168360 : EMBRYONIC LETHAL, ABNORMAL VISION, DROSOPHILA, HOMOLOG-LIKE 4; ELAVL4 168400 : PARASTREMMATIC DWARFISM *168440 : PARATHYMOSIN; PTMS *168450 : PARATHYROID HORMONE; PTH ^168460 : MOVED TO 145001 *168461 : CYCLIN D1; CCND1 *168468 : PARATHYROID HORMONE RECEPTOR 1; PTHR1 *168470 : PARATHYROID HORMONE-LIKE HORMONE; PTHLH #168500 : PARIETAL FORAMINA; PFM 168550 : PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA #168600 : PARKINSON DISEASE; PD #168601 : PARKINSON DISEASE, AUTOSOMAL DOMINANT LEWY BODY *168605 : PARKINSONISM WITH ALVEOLAR HYPOVENTILATION AND MENTAL DEPRESSION #168610 : PALLIDOPONTONIGRAL DEGENERATION; PPND 168710 : PAROTID PROLINE-RICH SALIVARY PROTEIN Pc *168730 : PROLINE-RICH PROTEIN, HaeIII SUBFAMILY, 1; PRH1 *168790 : PROLINE-RICH PROTEIN, HaeIII SUBFAMILY, 2; PRH2 168800 : PAROTIDOMEGALY, HEREDITARY BILATERAL *168810 : PROLINE-RICH PROTEIN, BstNI SUBFAMILY, 2; PRB2 *168820 : PARAOXONASE 1; PON1 168830 : PASSOVOY FACTOR *168840 : PROLINE-RICH PROTEIN, BstNI SUBFAMILY, 3; PRB3 168850 : PATELLA APLASIA, COXA VARA, AND TARSAL SYNOSTOSIS *168860 : PATELLA APLASIA-HYPOPLASIA; PTLAH 168885 : PAROXYSMAL TONIC UPGAZE, BENIGN CHILDHOOD, WITH ATAXIA *168890 : PARVALBUMIN; PVALB *168900 : PATELLA, CHONDROMALACIA OF *169000 : PATELLA, FAMILIAL RECURRENT DISLOCATION OF #169100 : CHAR SYNDROME #169150 : PATTERNED DYSTROPHY OF RETINAL PIGMENT EPITHELIUM 169170 : PATTERSON PSEUDOLEPRECHAUNISM SYNDROME *169190 : PCTAIRE PROTEIN KINASE 3; PCTK3 169200 : PECHET FACTOR DEFICIENCY 169300 : PECTUS EXCAVATUM *169400 : PELGER-HUET ANOMALY *169500 : LEUKODYSTROPHY, ADULT-ONSET, AUTOSOMAL DOMINANT *169545 : PELVIC LIPOMATOSIS WITH CROSSED RENAL ECTOPIA 169550 : PELVIS-SHOULDER DYSPLASIA #169600 : BENIGN CHRONIC PEMPHIGUS; BCPM 169610 : PEMPHIGUS VULGARIS, FAMILIAL *169615 : DESMOGLEIN 3; DSG3 *169700 : PEPSINOGEN; PG *169710 : PEPSINOGEN 3, GROUP I; PGA3 *169720 : PEPSINOGEN 4, GROUP I; PGA4 *169730 : PEPSINOGEN 5, GROUP I; PGA5 *169740 : PEPSINOGEN C *169800 : PEPTIDASE A; PEPA *169900 : PEPTIDASE B; PEPB *170000 : PEPTIDASE C; PEPC *170100 : PEPTIDASE D; PEPD *170200 : PEPTIDASE E; PEPE *170250 : PEPTIDASE S; PEPS *170260 : TRANSPORTER, ATP-BINDING CASSETTE, MAJOR HISTOCOMPATIBILITY COMPLEX, 1; TAP1 *170261 : TRANSPORTER, ATP-BINDING CASSETTE, MAJOR HISTOCOMPATIBILITY COMPLEX, 2; TAP2 *170270 : PEPTIDYLGLYCINE ALPHA-AMIDATING MONOOXYGENASE; PAM *170280 : PERFORIN 1; PRF1 *170285 : PERICENTRIN 1; PCNT1 *170290 : PERILIPIN; PLIN ^170300 : MOVED TO 142680 #170390 : PERIODIC PARALYSIS, POTASSIUM-SENSITIVE CARDIODYSRHYTHMIC TYPE #170400 : HYPOKALEMIC PERIODIC PARALYSIS; HOKPP #170500 : HYPERKALEMIC PERIODIC PARALYSIS; HYPP 170600 : NORMOKALEMIC PERIODIC PARALYSIS *170650 : PERIODONTITIS, JUVENILE; JPD 170700 : PERIPHERAL DYSOSTOSIS *170710 : PERIPHERIN; PRPH *170715 : PERIPHERAL MYELIN PROTEIN 2; PMP2 170900 : PERNICIOUS ANEMIA ^170950 : REMOVED FROM DATABASE 170980 : PERONEAL NERVE, ACCESSORY DEEP 170990 : PEROXIDASE, SALIVARY; SAPX *170993 : PEROXISOMAL MEMBRANE PROTEIN 3; PXMP3 *170995 : ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3; ABCD3 *170998 : PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-ALPHA; PPARA *171000 : PEYRONIE DISEASE *171050 : ATP-BINDING CASSETTE, SUBFAMILY B, MEMBER 1; ABCB1 *171060 : ATP-BINDING CASSETTE, SUBFAMILY B, MEMBER 4; ABCB4 171100 : PHAGOCYTOSIS, PLASMA-RELATED DEFECT IN *171150 : SULFOTRANSFERASE FAMILY 1A, PHENOL-PREFERRING, MEMBER 1; SULT1A1 *171190 : PHENYLETHANOLAMINE N-METHYLTRANSFERASE; PNMT *171200 : PHENYLTHIOCARBAMIDE TASTING #171300 : PHEOCHROMOCYTOMA 171350 : PHEOCHROMOCYTOMA, FAMILIAL EXTRAADRENAL #171400 : MULTIPLE ENDOCRINE NEOPLASIA, TYPE II; MEN2 171420 : PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME 171450 : PHLEBECTASIA OF LIPS 171480 : PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA *171490 : PHOSDUCIN; PDC *171500 : ACID PHOSPHATASE 1, SOLUBLE; ACP1 *171640 : PHOSPHATASE, ACID, TYPE 5, TARTRATE-RESISTANT; ACP5 *171650 : ACID PHOSPHATASE 2, LYSOSOMAL; ACP2 171660 : PHOSPHATASE, ACID, OF TISSUES 171700 : ALKALINE PHOSPHATASE, BLOOD GROUP-ASSOCIATED *171720 : ALKALINE PHOSPHATASE, ELEVATED SERUM *171740 : ALKALINE PHOSPHATASE, INTESTINAL; ALPI *171750 : ALKALINE PHOSPHATASE, INTESTINAL, FETAL FORM *171760 : ALKALINE PHOSPHATASE, LIVER; ALPL *171790 : PHOSPHATASE, PROSTATE-SPECIFIC ACID; ACPP *171800 : ALKALINE PHOSPHATASE, PLACENTAL; ALPP *171810 : ALKALINE PHOSPHATASE, PLACENTAL-LIKE 2; ALPPL2 *171820 : PHOSPHATASE, SALIVARY ACID, A; SACP; ACPS *171830 : PHOSPHATASE, SALIVARY ACID, B *171833 : PHOSPHATIDYLINOSITOL 3-KINASE, REGULATORY, 1; PIK3R1 *171834 : PHOSPHATIDYLINOSITOL 3-KINASE, CATALYTIC, ALPHA; PIK3CA *171835 : 6-@PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE 2; PFKFB2 *171840 : PHOSPHOFRUCTOKINASE, PLATELET TYPE; PFKP 171850 : PHOSPHOFRUCTOKINASE, RED CELL *171860 : PHOSPHOFRUCTOKINASE, LIVER TYPE; PFKL *171880 : PHOSPHOFRUCTOKINASE X; PFKX *171885 : PHOSPHODIESTERASE 7A, cAMP-SPECIFIC, HIGH-AFFINITY; PDE7A *171890 : PHOSPHODIESTERASE 1A; PDE1A *171891 : PHOSPHODIESTERASE 1B; PDE1B *171900 : PHOSPHOGLUCOMUTASE 1; PGM1 *172000 : PHOSPHOGLUCOMUTASE 2; PGM2 *172100 : PHOSPHOGLUCOMUTASE 3; PGM3 172110 : PHOSPHOGLUCOMUTASE 4 *172150 : 6-@PHOSPHOGLUCONOLACTONASE DEFICIENCY *172200 : 6-@PHOSPHOGLUCONATE DEHYDROGENASE, ERYTHROCYTE; PGD *172250 : PHOSPHOGLYCERATE MUTASE 1; PGAM1 *172270 : PHOSPHOGLYCERATE KINASE 2; PGK2 *172280 : PHOSPHOGLYCOLATE PHOSPHATASE; PGP 172290 : PHOSPHOGLYCOPROTEIN 1; PGP1 ^172300 : MOVED TO 171860 *172400 : GLUCOSE-6-PHOSPHATE ISOMERASE; GPI *172405 : PHOSPHOLAMBAN; PLN *172410 : PHOSPHOLIPASE A2, GROUP IB; PLA2G1B *172411 : PHOSPHOLIPASE A2, GROUP IIA; PLA2G2A *172420 : PHOSPHOLIPASE C, GAMMA-1; PLCG1 *172425 : PHOSPHOLIPID TRANSFER PROTEIN; PLTP *172430 : ENOLASE 1; ENO1 *172439 : PHOSPHORIBOSYLAMINOIMIDAZOLE CARBOXYLASE; PAICS *172450 : PHOSPHORIBOSYLPYROPHOSPHATE AMIDOTRANSFERASE; PPAT *172460 : METHYLENETETRAHYDROFOLATE DEHYDROGENASE 1; MTHFD1 *172470 : PHOSPHORYLASE KINASE, MUSCLE, GAMMA-1; PHKG1 *172471 : PHOSPHORYLASE KINASE, TESTIS/LIVER, GAMMA-2; PHKG2 *172480 : PHOSPHOSERINE PHOSPHATASE; PSPH *172490 : PHOSPHORYLASE KINASE, BETA SUBUNIT; PHKB 172500 : PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRAL DYSFUNCTION #172700 : PICK DISEASE OF BRAIN #172800 : PIEBALD TRAIT; PBT 172850 : PIEBALD TRAIT WITH NEUROLOGIC DEFECTS *172860 : PIGMENT EPITHELIUM-DERIVED FACTOR; PEDF 172870 : PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY; PPCRA 172880 : PIERRE ROBIN SYNDROME AND OLIGODACTYLY *172900 : PIGMENTED PURPURIC ERUPTION 173000 : PILONIDAL SINUS #173100 : PITUITARY DWARFISM DUE TO ISOLATED GROWTH HORMONE DEFICIENCY, AUTOSOMAL DOMINANT *173110 : POU DOMAIN, CLASS 1, TRANSCRIPTION FACTOR 1; POU1F1 *173120 : SECRETORY GRANULE NEUROENDOCRINE PROTEIN 1; SGNE1 *173200 : PITYRIASIS RUBRA PILARIS *173310 : PROGESTAGEN-ASSOCIATED ENDOMETRIAL PROTEIN; PAEP *173320 : PLACENTAL RIBONUCLEASE INHIBITOR; RNH *173321 : PROTEASE INHIBITOR 6; PI6 *173325 : JUNCTION PLAKOGLOBIN; JUP *173335 : ECTONUCLEOTIDE PYROPHOSPHATASE/PHOSPHODIESTERASE 1; ENPP1 173340 : PLASMINOGEN-LIKE; PLGL *173350 : PLASMINOGEN; PLG *173360 : PLASMINOGEN ACTIVATOR INHIBITOR 1; PAI1 *173370 : PLASMINOGEN ACTIVATOR, TISSUE; PLAT *173390 : PLASMINOGEN ACTIVATOR INHIBITOR, TYPE 2; PAI2 *173391 : PLASMINOGEN ACTIVATOR RECEPTOR, UROKINASE-TYPE; PLAUR *173393 : PLATELET-ACTIVATING FACTOR RECEPTOR; PTAFR 173395 : PLATELET ADENYLATE CYCLASE ACTIVITY 173400 : PLATELET AGGREGATION, SPONTANEOUS *173410 : PLATELET-DERIVED GROWTH FACTOR RECEPTOR, BETA; PDGFRB 173420 : PLATELET DISORDER, UNDEFINED *173430 : PLATELET-DERIVED GROWTH FACTOR, ALPHA POLYPEPTIDE; PDGFA *173445 : PLATELET-ENDOTHELIAL CELL ADHESION MOLECULE 1; PECAM1 173450 : PLATELET FACTOR 3 DEFICIENCY *173460 : PLATELET FACTOR 4; PF4 *173461 : PLATELET FACTOR 4, VARIANT 1; PF4V1 *173470 : INTEGRIN, BETA-3; ITGB3 *173490 : PLATELET-DERIVED GROWTH FACTOR RECEPTOR, ALPHA; PDGFRA *173500 : PLATELET GROUPS--Ko SYSTEM; HPA-2 *173510 : CD36 ANTIGEN; CD36 *173511 : PLATELET GLYCOPROTEIN V; GP5 *173515 : GLYCOPROTEIN IX, PLATELET; GP9 *173540 : PLATELET GROUPS--Pl(E) SYSTEM 173560 : PLATELET MEMBRANE FLUIDITY; PMF *173570 : PLECKSTRIN; PLEK 173580 : PLATELET RESPONSIVENESS TO ADRENALINE, DEPRESSED 173590 : PLATELET SIGNAL PROCESSING DEFECT *173600 : PNEUMOTHORAX, SPONTANEOUS *173610 : SELECTIN P; SELP *173650 : POIKILODERMA, HEREDITARY ACROKERATOTIC 173700 : POIKILODERMA, HEREDITARY SCLEROSING 173750 : POLAND-MOEBIUS SYNDROME 173800 : POLAND SYNDROME *173850 : POLIOVIRUS RECEPTOR; PVR *173865 : POLYADENYLATE-BINDING PROTEIN-LIKE 1; PABPL1 *173870 : ADP-RIBOSYLTRANSFERASE; ADPRT ^173871 : MOVED TO 173870 *173880 : POLYMERIC IMMUNOGLOBULIN RECEPTOR; PIGR #173900 : POLYCYSTIC KIDNEYS *173910 : POLYCYSTIC KIDNEY DISEASE 2; PKD2 *174000 : MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1 *174050 : POLYCYSTIC LIVER DISEASE; PCLD 174100 : POLYDACTYLY, IMPERFORATE ANUS, AND VERTEBRAL ANOMALIES #174200 : POLYDACTYLY, POSTAXIAL, TYPE A1 174300 : POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP 174310 : POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA #174400 : POLYDACTYLY, PREAXIAL I *174500 : POLYDACTYLY, PREAXIAL II; PPD2 *174600 : POLYDACTYLY, PREAXIAL III #174700 : POLYDACTYLY, PREAXIAL IV *174750 : POLYKARYOCYTOSIS INDUCER; FUSE *174760 : POLYMERASE, DNA, BETA; POLB *174761 : POLYMERASE, DNA, DELTA-1, CATALYTIC SUBUNIT; POLD1 *174762 : POLYMERASE, DNA, EPSILON; POLE *174763 : POLYMERASE, DNA, GAMMA; POLG *174770 : ACTINIC PRURIGO #174800 : MCCUNE-ALBRIGHT SYNDROME; MAS #174810 : POLYOSTOTIC OSTEOLYTIC DYSPLASIA, HEREDITARY EXPANSILE; HEPOD *174880 : LYMPHOCYTE CYTOSOL POLYPEPTIDE, 100-KD #174900 : POLYPOSIS, JUVENILE INTESTINAL ^175000 : MOVED TO 174900 *175020 : POLYPOSIS, GASTRIC 175050 : POLYPOSIS, GENERALIZED JUVENILE, WITH PULMONARY ARTERIOVENOUS MALFORMATION *175100 : ADENOMATOUS POLYPOSIS OF THE COLON; APC #175200 : PEUTZ-JEGHERS SYNDROME; PJS 175400 : POLYPOSIS, INTESTINAL, SCATTERED AND DISCRETE 175450 : POLYPOSIS, INTESTINAL, WITH MULTIPLE EXOSTOSES 175500 : POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES 175505 : POLYPOSIS OF GASTRIC FUNDUS WITHOUT POLYPOSIS COLI 175510 : POLYPS, MULTIPLE AND RECURRENT INFLAMMATORY FIBROID, GASTROINTESTINAL *175690 : POLYSYNDACTYLY, CROSSED #175700 : GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS 175750 : POPLITEAL CYST *175780 : PORENCEPHALY, FAMILIAL *175800 : POROKERATOSIS OF MIBELLI 175850 : POROKERATOSIS PLANTARIS, PALMARIS, ET DISSEMINATA *175860 : POROKERATOSIS PUNCTATA PALMARIS ET PLANTARIS; PPPP *175900 : POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC; DSAP *176000 : PORPHYRIA, ACUTE INTERMITTENT *176010 : PORPHYRIA, CHESTER TYPE; PORC 176090 : PORPHYRIA CUTANEA TARDA, TYPE I *176100 : PORPHYRIA CUTANEA TARDA #176200 : PORPHYRIA VARIEGATA 176240 : POSTAXIAL OLIGODACTYLY, TETRAMELIC 176250 : POSTERIOR COLUMN ATAXIA *176256 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAW-RELATED SUBFAMILY, MEMBER 2; KCNC2 *176257 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAKER-RELATED SUBFAMILY, MEMBER 6; KCNA6 *176258 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAW-RELATED SUBFAMILY, MEMBER 1; KCNC1 *176260 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAKER-RELATED SUBFAMILY, MEMBER 1; KCNA1 *176261 : POTASSIUM CHANNEL, VOLTAGE-GATED, ISK-RELATED SUBFAMILY, MEMBER 1; KCNE1 *176262 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAKER-RELATED SUBFAMILY, MEMBER 2; KCNA2 *176263 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAKER-RELATED SUBFAMILY, MEMBER 3; KCNA3 *176264 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAW-RELATED SUBFAMILY, MEMBER 3; KCNC3 *176265 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAW-RELATED SUBFAMILY, MEMBER 4; KCNC4 *176266 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAKER-RELATED SUBFAMILY, MEMBER 4; KCNA4 *176267 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAKER-RELATED SUBFAMILY, MEMBER 5; KCNA5 *176268 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAKER-RELATED SUBFAMILY, MEMBER 7; KCNA7 ^176269 : MOVED TO 176266 #176270 : PRADER-WILLI SYNDROME; PWS *176290 : DELTA, DROSOPHILA, HOMOLOG-LIKE 1; DLK1 *176300 : TRANSTHYRETIN; TTR #176305 : PREAXIAL DEFICIENCY, POSTAXIAL POLYDACTYLY, AND HYPOSPADIAS *176310 : PRE-B-CELL LEUKEMIA TRANSCRIPTION FACTOR 1; PBX1 *176311 : PRE-B-CELL LEUKEMIA TRANSCRIPTION FACTOR 2; PBX2 *176312 : PRE-B-CELL LEUKEMIA TRANSCRIPTION FACTOR 3; PBX3 *176385 : PREGNANCY-ASSOCIATED PLASMA PROTEIN A; PAPPA *176390 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 1; PSG1 *176391 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 2; PSG2 *176392 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 3; PSG3 *176393 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 4; PSG4 *176394 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 5; PSG5 *176395 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 6; PSG6 *176396 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 7; PSG7 *176397 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 8; PSG8 *176398 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 9; PSG9 *176399 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 10; PSG10 *176400 : PRECOCIOUS PUBERTY *176401 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 11; PSG11 #176410 : PRECOCIOUS PUBERTY, MALE-LIMITED *176420 : PREGNANCY ZONE PROTEIN; PZP *176430 : PREMATURE CHROMATID SEPARATION ^176440 : MOVED TO 311360 #176450 : CURRARINO SYNDROME #176500 : DEMENTIA, FAMILIAL BRITISH; FBD *176590 : PROFILIN 2; PFN2 176600 : PRESENILE DEMENTIA, KRAEPELIN TYPE *176610 : PROFILIN 1; PFN1 176620 : PRIAPISM, FAMILIAL IDIOPATHIC 176630 : PRIMARY RELEASE DISORDER OF PLATELETS *176635 : PRIMASE POLYPEPTIDE 1; PRIM1 *176636 : PRIMASE POLYPEPTIDE 2A; PRIM2A *176640 : PRION PROTEIN; PRNP 176670 : PROGERIA *176680 : PRIMED LYMPHOCYTE TEST 1; PLT1 176690 : PROGEROID SHORT STATURE WITH PIGMENTED NEVI *176700 : PROGNATHISM, MANDIBULAR *176705 : PROHIBITIN; PHB *176710 : PROCOLLAGEN-PROLINE,2-OXOGLUTARATE-4-DIOXYGENASE, ALPHA SUBUNIT, ISOFORM 1; P4HA1 *176720 : PROLACTIN-INDUCIBLE PROTEIN; PIP *176730 : INSULIN; INS *176740 : PROLIFERATING CELL NUCLEAR ANTIGEN; PCNA *176741 : PROLIFERATION-RELATED Ki-67 ANTIGEN; MKI67 *176760 : PROLACTIN; PRL *176761 : PROLACTIN RECEPTOR; PRLR *176763 : PEROXIREDOXIN 1; PRDX1 *176770 : PROLINE-NEGATIVE AUXOTROPH OF HAMSTER, COMPLEMENTATION OF; PROA 176780 : PROLAPSE OF VAGINA AND RECTUM *176785 : PROLYLCARBOXYPEPTIDASE; PRCP *176790 : PROCOLLAGEN-PROLINE,2-OXOGLUTARATE-4-DIOXYGENASE, BETA SUBUNIT; P4HB *176793 : PRO-MELANIN-CONCENTRATING HORMONE-LIKE 1; PMCHL1 *176794 : PRO-MELANIN-CONCENTRATING HORMONE-LIKE 2; PMCHL2 *176795 : PRO-MELANIN-CONCENTRATING HORMONE; PMCH *176797 : ZINC FINGER PROTEIN 145; ZNF145 176800 : PRONATION-SUPINATION OF THE FOREARM, IMPAIRMENT OF *176801 : PROSAPOSIN; PSAP *176802 : PROSTAGLANDIN E RECEPTOR 1, EP1 SUBTYPE; PTGER1 *176803 : PROSTAGLANDIN D2 SYNTHASE, BRAIN; PTGDS *176804 : PROSTAGLANDIN E RECEPTOR 2, EP2 SUBTYPE; PTGER2 *176805 : PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 1; PTGS1 *176806 : PROSTAGLANDIN E RECEPTOR 3, EP3 SUBTYPE; PTGER3 #176807 : PROSTATE CANCER *176820 : KALLIKREIN 3; KLK3 *176830 : PROOPIOMELANOCORTIN; POMC *176842 : PROTEASOME SUBUNIT, ALPHA-TYPE, 2; PSMA2 *176843 : PROTEASOME SUBUNIT, ALPHA-TYPE, 3; PSMA3 *176844 : PROTEASOME SUBUNIT, ALPHA-TYPE, 5; PSMA5 *176845 : PROTEASOME COMPONENT 8; PSC8 *176846 : PROTEASOME COMPONENT-9; PSC9 *176847 : PROTEASOME SUBUNIT, BETA-TYPE, 10; PSMB10 *176851 : PROTEIN CARBOXYL METHYLTRANSFERASE 1; PCMT1 *176860 : PROTEIN C DEFICIENCY, CONGENITAL THROMBOTIC DISEASE DUE TO *176870 : ALPHA-1 MICROGLOBULIN/BIKUNIN PRECURSOR; AMBP *176871 : PROTEIN KINASE, INTERFERON-INDUCIBLE DOUBLE-STRANDED RNA-ACTIVATED; PRKR *176872 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE 1; MAP2K1 *176873 : CELL DIVISION CYCLE 2-LIKE 1; CDC2L1 ^176874 : MOVED TO 114085 *176875 : PROTEIN PHOSPHATASE 1, CATALYTIC SUBUNIT, ALPHA ISOFORM; PPP1CA *176876 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 11; PTPN11 *176877 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 3; PTPN3 *176878 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 4; PTPN4 *176879 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 5; PTPN5 *176880 : PROTEIN S, ALPHA; PROS1 *176882 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, BETA; PTPRB *176883 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 6; PTPN6 *176884 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, ALPHA; PTPRA *176885 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 1; PTPN1 *176886 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, GAMMA; PTPRG *176887 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 2; PTPN2 *176888 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, MU; PTPRM *176889 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 7; PTPN7 *176891 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, ZETA-1; PTPRZ1 *176892 : PROTEIN KINASE, cAMP-DEPENDENT, CATALYTIC, BETA; PRKACB *176893 : PROTEIN KINASE, cAMP-DEPENDENT, CATALYTIC, GAMMA; PRKACG *176894 : PROTEIN KINASE, cGMP-DEPENDENT, REGULATORY, TYPE I; PRKG1 *176895 : PROTEIN Z; PROZ 176900 : PROTEOLYTIC CAPACITY OF PLASMA *176910 : PROTEIN KINASE, cAMP-DEPENDENT, REGULATORY, TYPE II, ALPHA; PRKAR2A *176911 : PROTEIN KINASE, cAMP-DEPENDENT, REGULATORY, TYPE I, BETA; PRKAR1B *176912 : PROTEIN KINASE, cAMP-DEPENDENT, REGULATORY, TYPE II, BETA; PRKAR2B *176914 : PROTEIN PHOSPHATASE 1, CATALYTIC SUBUNIT, GAMMA ISOFORM; PPP1CC *176915 : PROTEIN PHOSPHATASE 2A, CATALYTIC SUBUNIT, ALPHA ISOFORM; PPP2CA *176916 : PROTEIN PHOSPHATASE 2A, CATALYTIC SUBUNIT, BETA ISOFORM; PPP2CB 176920 : PROTEUS SYNDROME *176930 : COAGULATION FACTOR II; F2 *176940 : S100 CALCIUM-BINDING PROTEIN A1; S100A1 *176941 : PROTEIN-TYROSINE KINASE 2; TYK2 *176942 : FPS/FES-RELATED TYROSINE KINASE; FER *176943 : FIBROBLAST GROWTH FACTOR RECEPTOR 2; FGFR2 ^176944 : MOVED TO 134935 *176945 : EPHRIN RECEPTOR EphA8; EPHA8 *176946 : EPHRIN RECEPTOR EphA2; EPHA2 *176947 : ZETA-CHAIN-ASSOCIATED PROTEIN KINASE; ZAP70 *176948 : MITOGEN-ACTIVATED PROTEIN KINASE 1; MAPK1 *176949 : MITOGEN-ACTIVATED PROTEIN KINASE 4; MAPK4 *176950 : PROTHROMBIN CONVERSION DEFECT, FAMILIAL *176960 : PROTEIN KINASE C, ALPHA; PRKCA *176970 : PROTEIN KINASE C, BETA-1; PRKCB1 *176975 : PROTEIN KINASE C, EPSILON; PRKCE *176977 : PROTEIN KINASE C, DELTA; PRKCD *176980 : PROTEIN KINASE C, GAMMA; PRKCG *176981 : GUANINE NUCLEOTIDE-BINDING PROTEIN, BETA-2-LIKE 1; GNB2L1 *176982 : PROTEIN KINASE C, ZETA FORM; PRKCZ *176990 : S100 CALCIUM-BINDING PROTEIN, BETA; S100B *176991 : S100 CALCIUM-BINDING PROTEIN A5; S100A5 *176992 : S100 CALCIUM-BINDING PROTEIN A3; S100A3 *176993 : S100 CALCIUM-BINDING PROTEIN A2; S100A2 *177000 : PROTOPORPHYRIA, ERYTHROPOIETIC *177010 : PROTEASE INHIBITOR 7; PI7 *177015 : PROTEIN SERINE KINASE H1; PSKH1 *177020 : PROTEINASE 3; PRTN3 ^177030 : MOVED TO 176880 *177040 : PROTEOGLYCAN 1; PRG1 *177045 : PROTEASOME SUBUNIT, BETA-TYPE, 9; PSMB9 *177046 : PROTEASOME SUBUNIT, BETA-TYPE, 8; PSMB8 *177050 : PROTRUSIO ACETABULI *177060 : PROTEIN KINASE C SUBSTRATE, 80-KD, HEAVY CHAIN; PRKCSH *177061 : MYRISTOYLATED ALANINE-RICH PROTEIN KINASE C SUBSTRATE; MARCKS *177070 : PROTEIN 4.2, ERYTHROCYTIC; EPB42 *177075 : V-MAF AVIAN MUSCULOAPONEUROTIC FIBROSARCOMA ONCOGENE HOMOLOG; MAF 177100 : PRURITUS, HEREDITARY LOCALIZED 177150 : PSEUDOACHONDROPLASTIC DYSPLASIA I #177170 : PSEUDOACHONDROPLASTIC DYSPLASIA #177200 : LIDDLE SYNDROME 177300 : PSEUDOARTHROGRYPOSIS 177350 : PSEUDOATROPHODERMA COLLI *177400 : BUTYRYLCHOLINESTERASE; BCHE *177500 : CHOLINESTERASE, SERUM, 2; CHE2 177600 : PSEUDOCHOLINESTERASE, INCREASE IN PLASMA LEVEL OF 177650 : PSEUDOEXFOLIATION OF THE LENS 177700 : PSEUDOGLAUCOMA 177720 : PSEUDOHYPERKALEMIA, FAMILIAL, DUE TO RED CELL LEAK #177735 : PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT *177750 : PSEUDOMONILETHRIX 177800 : PSEUDOPAPILLEDEMA #177820 : PSEUDO-VON WILLEBRAND DISEASE #177850 : PSEUDOXANTHOMA ELASTICUM, AUTOSOMAL DOMINANT 177860 : PSEUDOXANTHOMA ELASTICUM, DOMINANT TYPE II *177900 : PSORIASIS SUSCEPTIBILITY 177980 : PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES 177990 : PTERYGIUM COLLI, ISOLATED 178000 : PTERYGIUM OF CONJUNCTIVA AND CORNEA 178110 : PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT *178200 : PTERYGIUM, ANTECUBITAL *178300 : PTOSIS, HEREDITARY CONGENITAL 1; PTOS1 178330 : PTOSIS, STRABISMUS, AND ECTOPIC PUPILS *178350 : PUBIC BONE DYSPLASIA 178370 : PULMONARY ATRESIA WITH VENTRICULAR SEPTAL DEFECT 178400 : PULMONARY EDEMA OF MOUNTAINEERS 178500 : PULMONARY FIBROSIS, IDIOPATHIC 178550 : PULMONARY HEMOSIDEROSIS #178600 : PULMONARY HYPERTENSION, PRIMARY; PPH1 178610 : PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL *178620 : SURFACTANT, PULMONARY-ASSOCIATED PROTEIN C; SFTPC *178630 : SURFACTANT, PULMONARY-ASSOCIATED PROTEIN A1; SFTPA1 *178635 : SURFACTANT, PULMONARY-ASSOCIATED PROTEIN D; SFTPD *178640 : SURFACTANT, PULMONARY-ASSOCIATED PROTEIN B; SFTPB *178642 : SURFACTANT, PULMONARY-ASSOCIATED PROTEIN A2; SFTPA2 178650 : PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHIC ABNORMALITIES 178651 : PULMONIC STENOSIS AND DEAFNESS 178800 : PUPIL, EGG-SHAPED 178900 : PUPILLARY MEMBRANE, PERSISTENCE OF *178990 : MATRIX METALLOPROTEINASE 7; MMP7 178995 : PRURITIC URTICARIAL PAPULES AND PLAQUES OF PREGNANCY; PUPPP 179000 : PURPURA SIMPLEX 179010 : PYLORIC STENOSIS, INFANTILE *179020 : PYRIDOXAL KINASE; PDXK *179030 : PYROPHOSPHATASE, INORGANIC; PP *179035 : PYRROLINE-5-CARBOXYLATE REDUCTASE 1; PYCR1 179040 : PYRUVATE KINASE 2; PK2 *179050 : PYRUVATE KINASE 3; PK3 *179060 : PYRUVATE DEHYDROGENASE, BETA POLYPEPTIDE; PDHB *179061 : PYRUVATE DEHYDROGENASE, E1-ALPHA POLYPEPTIDE, TESTIS-SPECIFIC FORM; PDHA2 *179080 : RAB GERANYLGERANYL TRANSFERASE, BETA SUBUNIT; RABGGTB ^179090 : MOVED TO 164730 *179095 : UBIQUITIN-CONJUGATING ENZYME E2B; UBE2B *179200 : RADIAL HEADS, POSTERIOR DISLOCATION OF 179250 : RADIAL HYPOPLASIA, TRIPHALANGEAL THUMBS, HYPOSPADIAS, AND MAXILLARY DIASTEMA 179270 : RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA 179280 : RADIAL-RENAL SYNDROME 179300 : RADIOULNAR SYNOSTOSIS 179400 : RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE *179410 : RADIXIN; RDX 179450 : RAGWEED SENSITIVITY *179490 : RAS-ASSOCIATED PROTEIN RAB3A; RAB3A 179500 : RAINDROP HYPOPIGMENTATION *179502 : RAP1, GTPase-GDP DISSOCIATION STIMULATOR 1; RAP1GDS1 *179503 : RAS-RELATED ASSOCIATED WITH DIABETES; RRAD *179505 : RAS HOMOLOG GENE FAMILY, MEMBER G; ARHG *179508 : RAS-ASSOCIATED PROTEIN RAB1; RAB1 *179509 : RAS-ASSOCIATED PROTEIN RAB2; RAB2 *179510 : RAS-ASSOCIATED PROTEIN RAB3B; RAB3B *179511 : RAS-ASSOCIATED PROTEIN RAB4; RAB4 *179512 : RAS-ASSOCIATED PROTEIN RAB5A; RAB5A *179513 : RAS-ASSOCIATED PROTEIN RAB6A; RAB6A *179514 : RAS-ASSOCIATED PROTEIN RAB5B; RAB5B *179520 : RAS-RELATED PROTEIN 1A; RAP1A *179530 : RAS-RELATED PROTEIN RAP1B; RAP1B *179540 : RAS-RELATED PROTEIN 2A; RAP2A *179541 : RAS-RELATED PROTEIN 2B; RAP2B *179550 : V-RAL SIMIAN LEUKEMIA VIRAL ONCOGENE HOMOLOG A; RALA *179551 : V-RAL SIMIAN LEUKEMIA VIRAL ONCOGENE HOMOLOG B; RALB *179555 : RAS SUPPRESSOR PROTEIN 1; RSU1 *179590 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, F; PTPRF *179600 : RAYNAUD DISEASE *179605 : RETINAL DEGENERATION, SLOW; RDS *179610 : EPHRIN RECEPTOR EphA1; EPHA1 *179611 : EPHRIN RECEPTOR EphA3; EPHA3 #179613 : RECOMBINANT CHROMOSOME 8 SYNDROME *179615 : RECOMBINATION-ACTIVATING GENE 1; RAG1 *179616 : RECOMBINATION-ACTIVATING GENE 2; RAG2 *179617 : RAD51, S. CEREVISIAE, HOMOLOG OF; RAD51 *179618 : RECOVERIN; RCV1 *179620 : RED BLOOD CELL ANTIGEN MER 2; MER2 *179650 : RED CELL PERMEABILITY DEFECT *179700 : RED CELL PHOSPHOLIPID DEFECT WITH HEMOLYSIS *179710 : CHROMOSOME CONDENSATION 1; CHC1 ^179715 : REMOVED FROM DATABASE *179730 : RELAXIN 1; RLN1 *179740 : RELAXIN 2; RLN2 *179755 : RENAL CELL CARCINOMA, PAPILLARY, 1 GENE; PRCC 179760 : RENAL CELL CARCINOMA 2; RCC2 179770 : RENAL CELL CARCINOMA 3; RCC3 *179780 : RENAL DIPEPTIDASE #179800 : RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT *179820 : RENIN; REN 179830 : RENAL TUBULAR ACIDOSIS, FAMILIAL PROXIMAL *179835 : REPLICATION PROTEIN A1, 70-KD; RPA1 *179836 : REPLICATION PROTEIN A2, 32-KD; RPA2 *179837 : REPLICATION PROTEIN A3, 14-KD; RPA3 *179838 : RESTIN; RSN 179840 : RETICULAR DYSTROPHY OF RETINAL PIGMENT EPITHELIUM 179850 : RETICULAR PIGMENTED ANOMALY OF FLEXURES *179900 : RETINAL APLASIA *180000 : RETINAL ARTERIES, TORTUOSITY OF *180020 : RETINAL CONE DEGENERATION 180040 : RETINAL DEGENERATION 3; RD3 *180050 : RETINAL DETACHMENT ^180060 : MOVED TO 152950 *180069 : RETINAL PIGMENT EPITHELIUM-SPECIFIC PROTEIN, 65-KD; RPE65 180070 : RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT *180071 : PHOSPHODIESTERASE 6A, cGMP-SPECIFIC, ROD, ALPHA; PDE6A *180072 : PHOSPHODIESTERASE 6B, cGMP-SPECIFIC, ROD, BETA; PDE6B *180073 : PHOSPHODIESTERASE 6G, cGMP-SPECIFIC, ROD, GAMMA; PDE6G 180080 : RETINAL VENOUS BEADING *180090 : RETINALDEHYDE-BINDING PROTEIN 1; RLBP1 #180100 : RETINITIS PIGMENTOSA 1; RP1 180102 : RETINITIS PIGMENTOSA 5; RP5 #180103 : RETINITIS PIGMENTOSA 8; RP8 *180104 : RETINITIS PIGMENTOSA 9; RP9 *180105 : RETINITIS PIGMENTOSA 10; RP10 *180190 : RETINOIC ACID RECEPTOR, GAMMA; RARG *180200 : RETINOBLASTOMA; RB1 *180201 : RETINOBLASTOMA-BINDING PROTEIN 1; RBBP1 *180202 : RETINOBLASTOMA-BINDING PROTEIN 2; RBBP2 *180203 : RETINOBLASTOMA-LIKE 2; RBL2 180210 : RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT *180220 : RETINOIC ACID RECEPTOR, BETA; RARB *180230 : RETINOIC ACID-BINDING PROTEIN, CELLULAR, TYPE I; CRABP1 *180231 : RETINOIC ACID-BINDING PROTEIN, CELLULAR, TYPE II; CRABP2 *180240 : RETINOIC ACID RECEPTOR, ALPHA; RARA *180245 : RETINOID X RECEPTOR, ALPHA; RXRA *180246 : RETINOID X RECEPTOR, BETA; RXRB *180247 : RETINOID X RECEPTOR, GAMMA; RXRG *180250 : RETINOL-BINDING PROTEIN 4; RBP4 *180260 : RETINOL-BINDING PROTEIN 1; RBP1 180270 : RETINOSCHISIS, AUTOSOMAL DOMINANT *180280 : RETINOL-BINDING PROTEIN 2; RBP2 *180290 : RETINOL-BINDING PROTEIN 3; RBP3 *180295 : RHABDOMYOSARCOMA, EMBRYONAL, 2; RMSE2 *180297 : RHESUS BLOOD GROUP-ASSOCIATED GLYCOPROTEIN; RHAG 180300 : RHEUMATOID ARTHRITIS 180330 : RHEUMATOID FACTOR IgM IDIOTYPES 180350 : RHEUMATOID NODULOSIS 180360 : RHINY *180370 : THIOSULFATE SULFURTRANSFERASE; TST *180380 : RHODOPSIN; RHO *180381 : RHODOPSIN KINASE; RHOK *180385 : LIM DOMAIN ONLY 2; LMO2 *180386 : LIM DOMAIN ONLY 3; LMO3 *180390 : RIBONUCLEOTIDE REDUCTASE, M2 SUBUNIT; RRM2 *180410 : RIBONUCLEOTIDE REDUCTASE, M1 SUBUNIT; RRM1 *180420 : RIBONUCLEIC ACID, RIBOSOMAL, 5S *180430 : RIBOSE 5-PHOSPHATE ISOMERASE A; RPIA *180435 : RIBONUCLEASE L; RNASEL *180440 : RIBONUCLEASE A FAMILY, 1; RNASE1 *180450 : RIBOSOMAL RNA 1; RNR1 *180451 : RIBOSOMAL RNA 2; RNR2 *180452 : RIBOSOMAL RNA 3; RNR3 *180453 : RIBOSOMAL RNA 4; RNR4 *180454 : RIBOSOMAL RNA 5; RNR5 *180460 : RIBOSOMAL PROTEIN S6; RPS6 ^180461 : MOVED TO 180472 ^180462 : MOVED TO 180472 *180463 : RIBOSOMAL PROTEIN S20A; RPS20A *180464 : RIBOSOMAL PROTEIN S20B; RPS20B *180465 : RIBOSOMAL PROTEIN S25; RPS25 *180466 : RIBOSOMAL PROTEIN L19; RPL19 *180467 : RIBOSOMAL PROTEIN L30; RPL30 *180468 : RIBOSOMAL PROTEIN L35A; RPL35A *180469 : RIBOSOMAL PROTEIN L36A-LIKE; RPL36AL *180470 : RIBOPHORIN I; RPN1 *180471 : RIBOSOMAL PROTEIN S11; RPS11 *180472 : RIBOSOMAL PROTEIN S17; RPS17 *180473 : RIBOSOMAL PROTEIN S18; RPS18 *180474 : RIBOSOMAL PROTEIN L22; RPL22 *180475 : RIBOSOMAL PROTEIN L12; RPL12 *180476 : RIBOSOMAL PROTEIN S13; RPS13 *180477 : RIBOSOMAL PROTEIN S21; RPS21 *180478 : RIBOSOMAL PROTEIN S3a; RPS3A *180479 : RIBOSOMAL PROTEIN L4; RPL4 *180480 : RIBULOSE 5-PHOSPHATE 3-EPIMERASE; RPE *180490 : RIBOPHORIN II; RPN2 #180500 : RIEGER SYNDROME, TYPE 1; RIEG1 *180510 : RIBOSOMAL PHOSPHOPROTEIN, LARGE, P0; RPLP0 *180520 : RIBOSOMAL PHOSPHOPROTEIN, LARGE, P1; RPLP1 *180530 : RIBOSOMAL PHOSPHOPROTEIN, LARGE, P2; RPLP2 *180535 : RIBOSOMAL PROTEIN S15; RPS15 *180540 : RIBONUCLEASE 1, SERUM 180550 : RING DERMOID OF CORNEA *180600 : RINGED HAIR *180610 : RLF PROTEIN INVOLVED IN ACTIVATION OF LMYC *180620 : TRANSFER RNA METHIONINE INITIATOR 1; TRMI1 *180621 : TRANSFER RNA METHIONINE INITIATOR 2; TRMI2 *180630 : DEAD/H BOX 5; DDX5 *180640 : TRANSFER RNA GLUTAMIC ACID; TRE #180645 : RNA, U17A SMALL NUCLEOLAR; RNU17A #180646 : RNA, U108 SMALL NUCLEOLAR; RNU108 *180647 : RNA, U107 SMALL NUCLEOLAR; RNU107 *180660 : POLYMERASE II, RNA, SUBUNIT A; POLR2A *180661 : POLYMERASE II, RNA, SUBUNIT B; POLR2B *180662 : POLYMERASE II, RNA, SUBUNIT I; POLR2I *180663 : POLYMERASE II, RNA, SUBUNIT C; POLR2C *180664 : POLYMERASE II, RNA, SUBUNIT E; POLR2E *180670 : RNA POLYMERASE III TRANSCRIPTIONAL UNITS *180680 : RNA, U1 SMALL NUCLEAR; RNU1 *180690 : RNA, U2 SMALL NUCLEAR; RNU2 *180691 : RNA, U5 SMALL NUCLEAR; RNU5 *180692 : RNA, U6 SMALL NUCLEAR; RNU6 *180700 : ROBINOW SYNDROME *180710 : RNA, U3 SMALL NUCLEAR; RNU3 ^180720 : MOVED TO 180680 *180721 : ROD OUTER SEGMENT PROTEIN 1; ROM1 180730 : ROMBO SYNDROME *180740 : SMALL NUCLEAR RIBONUCLEOPROTEIN, 70-KD; SNRP70 #180750 : ROBINOW-SORAUF SYNDROME *180800 : ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA ^180840 : MOVED TO 601625 #180849 : RUBINSTEIN SYNDROME 180850 : RUBINSTEIN-LIKE SYNDROME *180860 : RUSSELL-SILVER SYNDROME; RSS 180870 : RUVALCABA SYNDROME *180900 : RUTHERFURD SYNDROME *180901 : RYANODINE RECEPTOR 1; RYR1 *180902 : RYANODINE RECEPTOR 2; RYR2 *180903 : RYANODINE RECEPTOR 3; RYR3 *180910 : SALIVARY ESTERASE *180920 : SALIVARY GLANDS, ABSENCE OF 180930 : SALIVARY PROTEIN I; SAL-I 180940 : SALIVARY PROTEIN II; SAL-II *180950 : SALIVARY SUBSTANCE, CLOSTRIDIUM BOTULINUM TYPE *180960 : S-ADENOSYLHOMOCYSTEINE HYDROLASE; AHCY *180980 : S-ADENOSYLMETHIONINE DECARBOXYLASE; AMD1 *180989 : PROLINE-RICH PROTEIN, BstNI SUBFAMILY, 1; PRB1 *180990 : PROLINE-RICH PROTEIN, BstNI SUBFAMILY, 4; PRB4 181000 : SARCOIDOSIS 181010 : SALIVARY DUCT CALCULI #181030 : SALIVARY GLAND ADENOMA, PLEOMORPHIC *181031 : S-ANTIGEN; SAG *181035 : SARCOMA AMPLIFIED SEQUENCE; SAS 181180 : SAY SYNDROME 181200 : SC(1) TRAIT OF SALIVA 181250 : SCALP DEFECTS AND POSTAXIAL POLYDACTYLY 181270 : SCALP-EAR-NIPPLE SYNDROME 181300 : SCAPULA, CONTOUR OF VERTEBRAL BORDER OF #181350 : EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT; EDMD2 *181400 : AMYOTROPHY, SCAPULOPERONEAL *181405 : AMYOTROPHY, NEUROGENIC SCAPULOPERONEAL, NEW ENGLAND TYPE *181430 : SCAPULOPERONEAL MYOPATHY; SPM *181440 : SCHEUERMANN DISEASE #181450 : ULNAR-MAMMARY SYNDROME; UMS *181460 : SCHISTOSOMA MANSONI INFECTION, SUSCEPTIBILITY/RESISTANCE TO #181500 : SCHIZOPHRENIA; SCZD 181510 : SCHIZOPHRENIA 1; SCZD1 *181515 : SCHOLTE SYNDROME ^181520 : MOVED TO 104640 *181590 : SCL-INTERRUPTING LOCUS; SIL *181600 : SCLEROTYLOSIS; TYS 181700 : SCLEROCORNEA *181750 : SCLERODERMA, FAMILIAL PROGRESSIVE 181800 : SCOLIOSIS, IDIOPATHIC 182000 : SEBORRHEIC KERATOSES *182090 : SIMIAN SARCOMA-ASSOCIATED VIRUS-1/GIBBON APE LEUKEMIA VIRUS; SSAV1 *182098 : SECRETIN RECEPTOR; SCTR *182099 : SECRETIN; SCT *182100 : FUCOSYLTRANSFERASE 2; FUT2 *182115 : PLECKSTRIN HOMOLOGY, SEC7, AND COILED-COIL DOMAINS PROTEIN 1; PSCD1 *182120 : SECRETED PROTEIN, ACIDIC, CYSTEINE-RICH; SPARC *182125 : SEPIAPTERIN REDUCTASE; SPR *182128 : SERINE DEHYDRATASE; SDS *182131 : 5-@HYDROXYTRYPTAMINE RECEPTOR 1B; HTR1B *182132 : 5-@HYDROXYTRYPTAMINE RECEPTOR 1E; HTR1E *182133 : 5-@HYDROXYTRYPTAMINE RECEPTOR 1D; HTR1D *182134 : 5-@HYDROXYTRYPTAMINE RECEPTOR 1F; HTR1F *182135 : 5-@HYDROXYTRYPTAMINE RECEPTOR 2A; HTR2A *182137 : 5-@HYDROXYTRYPTAMINE RECEPTOR 7; HTR7 *182138 : SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, SEROTONIN), MEMBER 4; SLC6A4 *182139 : 5-@HYDROXYTRYPTAMINE RECEPTOR 3A; HTR3A *182140 : SEMENOGELIN; SEMG *182141 : SEMENOGELIN II; SEMG2 ^182143 : MOVED TO 177040 *182144 : SERINE HYDROXYMETHYLTRANSFERASE, CYTOSOLIC; SHMT1 *182145 : SERUM PROTEIN POLYMORPHISM M-158 182150 : SIMOSA CRANIOFACIAL SYNDROME *182160 : SIALOPHORIN; SPN 182170 : SIDEROBLASTIC ANEMIA WITH ERYTHROCYTE DIMORPHISM *182175 : SIGNAL RECOGNITION PARTICLE, 19-KD; SRP19 *182180 : SIGNAL RECOGNITION PARTICLE RECEPTOR; SRPR 182190 : SINUS NODE DISEASE AND MYOPIA 182200 : SELLA TURCICA, BRIDGED ^182203 : MOVED TO 162643 *182205 : SEX HORMONE-BINDING GLOBULIN; SHBG 182210 : SHPRINTZEN OMPHALOCELE SYNDROME #182212 : SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME 182220 : SISTER CHROMATID EXCHANGE, FREQUENCY OF #182230 : SEPTOOPTIC DYSPLASIA *182250 : SINGLETON-MERTEN SYNDROME 182255 : SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION *182257 : PROTEINASE INHIBITOR 3; PI3 182260 : SLIPPED FEMORAL CAPITAL EPIPHYSES *182265 : SMALL PROLINE-RICH PROTEIN 1A; SPRR1A *182266 : SMALL PROLINE-RICH PROTEIN 1B; SPRR1B *182267 : SMALL PROLINE-RICH PROTEIN 2A; SPRR2A *182268 : SMALL PROLINE-RICH PROTEIN 2B; SPRR2B 182269 : SMALL PROLINE-RICH PROTEIN 2C; SPRR2C 182270 : SMELL KETONE COMPOUNDS, ABILITY TO *182271 : SMALL PROLINE-RICH PROTEIN 3; SPRR3 *182279 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE N; SNRPN *182280 : SMALL CELL CANCER OF THE LUNG *182281 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 1; SCYA1 *182282 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDES B AND B1; SNRPB *182283 : SMALL INDUCIBLE CYTOKINE A3; SCYA3 *182284 : SMALL INDUCIBLE CYTOKINE A4; SCYA4 *182285 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE A; SNRPA #182290 : SMITH-MAGENIS SYNDROME; SMS *182305 : SOLUTE CARRIER FAMILY 8, MEMBER 1; SLC8A1 *182307 : SOLUTE CARRIER FAMILY 9, ISOFORM A3; SLC9A3 *182308 : SOLUTE CARRIER FAMILY 17, MEMBER 1; SLC17A1 *182309 : SOLUTE CARRIER FAMILY 34, MEMBER 1; SLC34A1 *182310 : ATPase, Na+/K+ TRANSPORTING, ALPHA-1 POLYPEPTIDE; ATP1A1 *182330 : ATPase, Na+/K+ TRANSPORTING, BETA-1 POLYPEPTIDE; ATP1B1 *182331 : ATPase, Na+/K+ TRANSPORTING, BETA-2 POLYPEPTIDE; ATP1B2 *182340 : ATPase, Na+/K+ TRANSPORTING, ALPHA-2 POLYPEPTIDE; ATP1A2 *182350 : ATPase, Na+/K+ TRANSPORTING, ALPHA-3 POLYPEPTIDE; ATP1A3 *182360 : ATPase, Na+/K+ TRANSPORTING, ALPHA POLYPEPTIDE-LIKE 1; ATP1AL1 182370 : SODIUM-POTASSIUM-ATPase, BETA-POLYPEPTIDE-LIKE *182380 : SOLUTE CARRIER FAMILY 5 (SODIUM/GLUCOSE COTRANSPORTER), MEMBER 1; SLC5A1 *182381 : SOLUTE CARRIER FAMILY 5 (SODIUM/GLUCOSE COTRANSPORTER), MEMBER 2; SLC5A2 *182389 : SODIUM CHANNEL, NEURONAL TYPE I, ALPHA SUBUNIT; SCN1A *182390 : SODIUM CHANNEL, VOLTAGE-GATED, TYPE II, ALPHA-1 SUBUNIT; SCN2A1 *182391 : SODIUM CHANNEL, NEURONAL TYPE III, ALPHA SUBUNIT; SCN3A *182392 : SODIUM CHANNEL, VOLTAGE-GATED, TYPE VII, ALPHA SUBUNIT; SCN7A *182396 : SOLUTE CARRIER FAMILY 10 (SODIUM/BILE ACID COTRANSPORTER FAMILY), MEMBER 1; SLC10A1 182400 : SOMATOMEDIN, EMBRYONIC 182410 : SNEDDON SYNDROME *182450 : SOMATOSTATIN; SST *182451 : SOMATOSTATIN RECEPTOR 1; SSTR1 *182452 : SOMATOSTATIN RECEPTOR 2; SSTR2 *182453 : SOMATOSTATIN RECEPTOR 3; SSTR3 *182454 : SOMATOSTATIN RECEPTOR 4; SSTR4 *182455 : SOMATOSTATIN RECEPTOR 5; SSTR5 *182465 : SON DNA-BINDING PROTEIN; SON *182500 : SORBITOL DEHYDROGENASE; SORD *182520 : SORCIN; SRI *182530 : SON OF SEVENLESS, DROSOPHILA, HOMOLOG 1; SOS1 *182590 : TREFOIL FACTOR 2; TFF2 #182600 : SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A #182601 : SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4 182610 : SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION; SPERM 182690 : SPASTIC PARAPLEGIA, SENSORINEURAL DEAFNESS, MENTAL RETARDATION, AND PROGRESSIVE NEPHROPATHY 182700 : SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS *182790 : SPECTRIN, BETA, NONERYTHROCYTIC, 1; SPTBN1 182800 : SPASTIC PARAPLEGIA WITH ASSOCIATED EXTRAPYRAMIDAL SIGNS *182810 : SPECTRIN, ALPHA, NONERYTHROCYTIC 1; SPTAN1 182815 : SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA 182820 : SPASTIC PARAPLEGIA WITH PRECOCIOUS PUBERTY 182830 : SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA *182860 : SPECTRIN, ALPHA, ERYTHROCYTIC 1; SPTA1 *182870 : SPECTRIN, BETA, ERYTHROCYTIC; SPTB 182875 : SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, AND TRANSVERSE EARLOBE CREASE *182878 : OUTER DENSE FIBER OF SPERM TAILS 1; ODF1 ^182879 : MOVED TO 104776 *182880 : SPERM PROTAMINE P1; PRM1 182882 : SPERM PROTAMINE P4; PRM4 *182888 : ZONA PELLUCIDA GLYCOPROTEIN 2; ZP2 *182889 : ZONA PELLUCIDA GLYCOPROTEIN 3A; ZP3A *182890 : SPERM PROTAMINE P2; PRM2 *182891 : SPERMIDINE SYNTHASE; SRM ^182892 : MOVED TO 300105 *182900 : SPHEROCYTOSIS, HEREDITARY; HS *182920 : SPHEROID BODY MYOPATHY 182930 : SPHINCTER OF ODDI, FAMILIAL HYPERTROPHY OF 182940 : SPINA BIFIDA *182950 : SPINAL ARACHNOIDITIS #182960 : SPINAL MUSCULAR ATROPHY, DISTAL *182970 : SPINAL MUSCULAR ATROPHY, FACIOSCAPULOHUMERAL TYPE; FSHSMA *182980 : SPINAL MUSCULAR ATROPHY, PROXIMAL, ADULT TYPE 182990 : SPINAL INTRADURAL ARACHNOID CYSTS *183000 : SPINOCEREBELLAR ATAXIA AND PLAQUE-LIKE DEPOSITS 183020 : SPINAL MUSCULAR ATROPHY, SEGMENTAL *183050 : SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY ^183085 : MOVED TO 109150 #183086 : SPINOCEREBELLAR ATAXIA 6; SCA6 #183090 : SPINOCEREBELLAR ATAXIA 2; SCA2 183100 : SPINOCEREBELLAR ATROPHY WITH PUPILLARY PARALYSIS 183250 : SPLENIN 183300 : SPLENOGONADAL FUSION WITH LIMB DEFECTS AND MICROGNATHIA #183350 : SPLENOMEGALY WITH HYPERSPLENISM 183400 : SPLIT LOWER LIP 183500 : SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA *183600 : SPLIT-HAND/FOOT MALFORMATION 1; SHFM1 183700 : SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS 183800 : SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS 183802 : SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATIC DEFECTS 183840 : SPONDYLOARTHROPATHY, AUTOSOMAL DOMINANT 183849 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS 183850 : SPONDYLOEPIPHYSEAL DYSPLASIA WITH PUNCTATE CORNEAL DYSTROPHY #183900 : SPONDYLOEPIPHYSEAL DYSPLASIA, CONGENITAL TYPE 184000 : SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS 184095 : SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE *184100 : SPONDYLOEPIPHYSEAL DYSPLASIA TARDA 184200 : SPONDYLOLISTHESIS #184250 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE *184252 : SPONDYLOMETAPHYSEAL DYSPLASIA 184253 : SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE *184255 : SPONDYLOMETAPHYSEAL DYSPLASIA, 'CORNER FRACTURE' TYPE 184260 : SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA 184300 : SPONDYLOSIS, CERVICAL *184400 : SPRENGEL DEFORMITY *184420 : FARNESYLDIPHOSPHATE FARNESYLTRANSFERASE 1; FDFT1 *184429 : SRY-BOX 2; SOX2 *184430 : SRY-BOX 4; SOX4 184450 : STUTTERING, FAMILIAL PERSISTENT 184460 : STAPES ANKYLOSIS WITH BROAD THUMB AND TOES *184470 : STATHERIN; STATH #184500 : STEATOCYSTOMA MULTIPLEX 184510 : STEATOCYSTOMA MULTIPLEX WITH NATAL TEETH *184600 : CYSTATIN A; CSTA ^184601 : MOVED TO 601145 #184700 : POLYCYSTIC OVARY SYNDROME 1; PCOS1 184705 : STEINFELD SYNDROME *184745 : KIT LIGAND; KITLG ^184747 : MOVED TO 136351 *184753 : STEROID 5-ALPHA-REDUCTASE 1; SRD5A1 ^184754 : MOVED TO 201910 *184755 : STEROL CARRIER PROTEIN 2; SCP2 *184756 : STEROL REGULATORY ELEMENT-BINDING TRANSCRIPTION FACTOR 1; SREBF1 *184757 : NUCLEAR RECEPTOR SUBFAMILY 5, GROUP A, MEMBER 1; NR5A1 184800 : STERNUM, PREMATURE OBLITERATION OF SUTURES OF #184840 : STICKLER SYNDROME, TYPE III; STL3 184850 : STIFF MAN SYNDROME, HEREDITARY FORM OF *184900 : STIFF SKIN SYNDROME #185000 : STOMATOCYTOSIS I *185010 : STOMATOCYTOSIS II 185020 : STOMATOCYTOSIS, COLD-SENSITIVE *185050 : STORAGE POOL PLATELET DISEASE 185069 : STORM SYNDROME 185070 : STORMORKEN SYNDROME 185100 : STRABISMUS 185120 : STRATTON-PARKER SYNDROME *185200 : STRIAE DISTENSAE, FAMILIAL *185250 : MATRIX METALLOPROTEINASE 3; MMP3 *185260 : MATRIX METALLOPROTEINASE 10; MMP10 *185261 : MATRIX METALLOPROTEINASE 11; MMP11 185300 : STURGE-WEBER SYNDROME 185400 : SUBGLOTTIC BAR *185430 : CLUSTERIN; CLU *185440 : SUPPRESSOR OF TUMORIGENICITY 2; ST2 185450 : SUBLUXATION OF LENSES, LATE 185460 : SULFHEMOGLOBINEMIA, CONGENITAL *185470 : SUCCINATE DEHYDROGENASE COMPLEX, SUBUNIT B, IRON SULFUR PROTEIN; SDHB 185480 : SUPRABULBAR PARESIS, CONGENITAL *185490 : SUPEROXIDE DISMUTASE, EXTRACELLULAR; SOD3 #185500 : SUPRAVALVULAR AORTIC STENOSIS; SVAS *185510 : SURFACE ANTIGEN 5; S5 *185520 : SURFACE ANTIGEN 6; S6 *185535 : TUMOR-ASSOCIATED CALCIUM SIGNAL TRANSDUCER 1; TACSTD1 185540 : SURFACE ANTIGEN, GLYCOPROTEIN 75 *185560 : SURFACE ANTIGEN 8; S8 *185570 : SURFACE ANTIGEN 17; SA17; S9 *185580 : SURFACE ANTIGEN 22; S13 *185590 : SURFACE ANTIGEN 21; S14 ^185595 : REMOVED FROM DATABASE 185600 : SYMPHALANGISM OF TOES *185605 : SYNAPTOTAGMIN 1; SYT1 185610 : SURFACE POLYPEPTIDES, ANONYMOUS *185620 : SURFEIT 1; SURF1 *185630 : SURFEIT 2; SURF2 *185640 : RIBOSOMAL PROTEIN L7a; RPL7A *185641 : SURFEIT 5; SURF5 *185642 : SURFEIT 6; SURF6 185650 : SYMPHALANGISM, C. S. LEWIS TYPE *185660 : SURFEIT 4; SURF4 *185700 : SYMPHALANGISM, DISTAL 185750 : SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET #185800 : SYMPHALANGISM, PROXIMAL; SYM1 185860 : SYNAPTIC VESICLE PROTEIN 2; SV2 185861 : SYNAPTIC VESICLE PROTEIN 2B; SV2B *185880 : VESICLE-ASSOCIATED MEMBRANE PROTEIN 1; VAMP1 *185881 : VESICLE-ASSOCIATED MEMBRANE PROTEIN 2; VAMP2 *185900 : SYNDACTYLY, TYPE I #186000 : SYNDACTYLY, TYPE II #186100 : SYNDACTYLY, TYPE III 186200 : SYNDACTYLY, TYPE IV *186300 : SYNDACTYLY, TYPE V *186350 : SYNDACTYLY-POLYDACTYLY-EARLOBE SYNDROME *186355 : SYNDECAN 1; SDC1 *186357 : SYNDECAN 3; SDC3 *186360 : ANNEXIN A7; ANXA7 *186400 : SYNOSTOSES, TARSAL, CARPAL AND DIGITAL #186500 : MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1 *186550 : SYNOSTOSIS, CARPAL, WITH DYSPLASTIC ELBOW JOINTS AND BRACHYDACTYLY #186570 : TARSAL-CARPAL COALITION SYNDROME; TCC 186575 : SYNOVIAL CHONDROMATOSIS, FAMILIAL, WITH DWARFISM #186580 : SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES *186590 : SYNTAXIN 1A; STX1A *186591 : SYNTAXIN 4A; STX4A 186600 : SYRINGOMAS, MULTIPLE *186690 : CD3 ANTIGEN, ETA SUBUNIT; CD3H 186700 : SYRINGOMYELIA *186710 : T-CELL ACTIVATION ANTIGEN p250; TP250 *186711 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 7; TNFRSF7 *186720 : CD6 ANTIGEN; CD6 *186730 : T-CELL GLYCOPROTEIN CD8B; CD8B *186740 : CD3 ANTIGEN, GAMMA SUBUNIT; CD3G *186745 : TALIN; TLN 186750 : TALONAVICULAR COALITION *186760 : ANTIGEN CD28; CD28 *186770 : HOMEO BOX 11; HOX11 *186780 : CD3 ANTIGEN, ZETA SUBUNIT; CD3Z *186790 : CD3 ANTIGEN, DELTA SUBUNIT; CD3D *186810 : T-CELL ANTIGEN RECEPTOR, DELTA SUBUNIT; TCRD *186820 : T-CELL ANTIGEN CD7; CD7 *186830 : CD3 ANTIGEN, EPSILON SUBUNIT; CD3E *186845 : CD81 ANTIGEN; CD81 *186850 : TARSAL FUSION *186852 : PROTEASOME 26S SUBUNIT, ATPase, 3; PSMC3 *186854 : SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, TAURINE), MEMBER 6; SLC6A6 *186855 : T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA 2; TAL2 *186860 : T-CELL LEUKEMIA/LYMPHOMA 4; TCL4 *186880 : T-CELL ANTIGEN RECEPTOR, ALPHA SUBUNIT; TCRA *186890 : TEAR PROTEIN, ANODAL *186910 : CD8 ANTIGEN, ALPHA POLYPEPTIDE; CD8A ^186920 : REMOVED FROM DATABASE *186921 : LIM DOMAIN ONLY 1; LMO1 *186930 : T-CELL ANTIGEN RECEPTOR, BETA SUBUNIT; TCRB *186940 : CD4 ANTIGEN; CD4 *186945 : FK506-BINDING PROTEIN 1A; FKBP1A *186946 : FK506-BINDING PROTEIN 2; FKBP2 *186947 : FK506-BINDING PROTEIN 3; FKBP3 186950 : T-CELL SUBGROUPS, NON-HLA-LINKED *186960 : T-CELL LEUKEMIA/LYMPHOMA 1A; TCL1A *186970 : T-CELL ANTIGEN RECEPTOR, GAMMA SUBUNIT; TCRG *186973 : T-CELL TYROSINE KINASE EMT; EMT *186975 : T-COMPLEX-ASSOCIATED-TESTES-EXPRESSED 1; TCTE1 *186977 : T-COMPLEX-ASSOCIATED-TESTES-EXPRESSED 3; TCTE3 *186980 : T-COMPLEX 1; TCP1 *186982 : T-COMPLEX HOMOLOG TCP11; TCP11 *186990 : T-LYMPHOCYTE SURFACE CD2 ANTIGEN; CD2 *187000 : TEETH, ODD SHAPES OF ^187010 : MOVED TO 187011 *187011 : SMALL INDUCIBLE CYTOKINE A5; SCYA5 *187020 : T-COMPLEX LOCUS TCP10A; TCP10A; TCP10 187030 : T-COMPLEX LOCUS TCP10B; TCP10B *187040 : T-CELL ACUTE LYMPHOCYTIC LEUKEMIA 1; TAL1 187050 : TEETH PRESENT AT BIRTH 187100 : TEETH, SUPERNUMERARY *187260 : TELANGIECTASIA, HEREDITARY BENIGN *187270 : TELOMERE REVERSE TRANSCRIPTASE; TERT *187280 : TEMPERATURE SENSITIVITY COMPLEMENTATION, CELL CYCLE SPECIFIC, tsBN51; BN51T; TSBN51 *187290 : TEMPERATURE SENSITIVITY COMPLEMENTATION, CELL CYCLE SPECIFIC, H142; H142T #187300 : TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT *187310 : TEMPERATURE SENSITIVITY COMPLEMENTATION, CELL CYCLE SPECIFIC, K12 *187320 : TEMPERATURE SENSITIVITY COMPLEMENTATION, CELL CYCLE SPECIFIC, ts13; TS13 *187330 : TEMPERATURE SENSITIVITY COMPLEMENTATION, CELL CYCLE SPECIFIC, ts546; TS546 187340 : TEMPERATURE-SENSITIVE LETHAL MUTATION 187350 : TELECANTHUS 187360 : TEMPORAL ARTERITIS *187370 : TENDO CALCANEUS, SHORT *187380 : TENASCIN C; TNC 187390 : TENDONS, EXTENSOR, OF FINGERS, ANOMALOUS INSERTION OF *187395 : TERATOCARCINOMA-DERIVED GROWTH FACTOR 1; TDGF1 187400 : TESTICULAR TORSION *187410 : TERMINAL DEOXYNUCLEOTIDYLTRANSFERASE; TDT *187430 : TESTIS-SPECIFIC PROTEIN 1; TPX1 *187450 : TESTOSTERONE-BINDING BETA-GLOBULIN; TEBG #187500 : TETRALOGY OF FALLOT 187501 : TETRALOGY OF FALLOT AND GLAUCOMA 187510 : TETRAMELIC MONODACTYLY *187520 : TETRANECTIN; TNA 187550 : THALASSEMIA, BETA+, SILENT ALLELE #187600 : THANATOPHORIC DYSPLASIA; TD #187601 : THANATOPHORIC DYSPLASIA WITH KLEEBLATTSCHAEDEL *187650 : THEOPHYLLINE BIOTRANSFORMATION *187680 : THIOPURINE S-METHYLTRANSFERASE; TPMT *187700 : THIOREDOXIN; TXN 187750 : THORACIC DYSOSTOSIS, ISOLATED 187760 : THORACOLARYNGOPELVIC DYSPLASIA; TLPD 187770 : THORACOPELVIC DYSOSTOSIS *187790 : THREONYL-tRNA SYNTHETASE; TARS 187800 : GLANZMANN THROMBASTHENIA; GTA *187900 : THROMBASTHENIA-THROMBOCYTOPENIA, HEREDITARY *187930 : COAGULATION FACTOR II RECEPTOR; F2R 187940 : THROMBOCYTE B; THB #187950 : THROMBOCYTHEMIA, ESSENTIAL *188000 : THROMBOCYTOPENIA 2; THC2 188020 : THROMBOCYTOPENIA, CYCLIC #188025 : THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT 188030 : THROMBOCYTOPENIC PURPURA, AUTOIMMUNE 188035 : THROMBOGLOBULIN, BETA-2; TGB2 *188040 : THROMBOMODULIN; THBD #188050 : THROMBOPHILIA #188055 : THROMBOPHILIA DUE TO DEFICIENCY OF ACTIVATED PROTEIN C COFACTOR *188060 : THROMBOSPONDIN I; THBS1 *188061 : THROMBOSPONDIN II; THBS2 *188062 : THROMBOSPONDIN III; THBS3 *188070 : THROMBOXANE A2 RECEPTOR, PLATELET; TBXA2R 188100 : THUMB DEFORMITY 188150 : THUMB DEFORMITY AND ALOPECIA 188200 : THUMBNAILS, ABSENT 188201 : THUMBS, STIFF, WITH BRACHYDACTYLY TYPE A1 AND DEVELOPMENTAL DELAY *188230 : THY-1 T-CELL ANTIGEN; THY1 *188250 : THYMIDINE KINASE, MITOCHONDRIAL; TK2 *188300 : THYMIDINE KINASE, SOLUBLE; TK1 *188340 : THYMOCYTE ANTIGEN CD1C; CD1C *188345 : DEOXYTHYMIDYLATE KINASE; DTYMK *188350 : THYMIDYLATE SYNTHETASE; TYMS *188360 : THYMOCYTE ANTIGEN CD1B; CD1B *188370 : THYMOCYTE ANTIGEN CD1A; CD1A *188380 : THYMOPOIETIN; TMPO *188390 : PROTHYMOSIN, ALPHA; PTMA ^188395 : MOVED TO 300159 *188399 : THYMOSIN, BETA-10; TMSB10 *188400 : DIGEORGE SYNDROME; DGS *188410 : THYMOCYTE ANTIGEN CD1D; CD1D *188411 : THYMOCYTE ANTIGEN CD1E; CD1E *188450 : THYROGLOBULIN; TG 188455 : THYROGLOSSAL DUCT CYST, FAMILIAL 188470 : THYROID CARCINOMA, FOLLICULAR; FTC #188530 : THYROTROPIN, ALPHA CHAIN *188540 : THYROID-STIMULATING HORMONE, BETA CHAIN; TSHB *188545 : THYROTROPIN-RELEASING HORMONE RECEPTOR; TRHR #188550 : THYROID CARCINOMA, PAPILLARY *188555 : THYROID HORMONE-BINDING PROTEIN, CYTOSOLIC; THBP1 188560 : THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT #188570 : THYROID HORMONE RESISTANCE 188580 : THYROTOXIC PERIODIC PARALYSIS ^188590 : MOVED TO 190120 *188595 : THYROTROPH EMBRYONIC FACTOR; TEF 188600 : THYROXINE-BINDING GLOBULIN OF SERUM 188700 : TIBIA VARA 188740 : TIBIA, ABSENCE OF, WITH POLYDACTYLY *188770 : TIBIA, HYPOPLASIA OF, WITH POLYDACTYLY *188800 : TIBIAL TORSION, BILATERAL MEDIAL *188825 : TISSUE INHIBITOR OF METALLOPROTEINASE 2; TIMP2 *188826 : TISSUE INHIBITOR OF METALLOPROTEINASE 3; TIMP3 *188830 : PROTEIN KINASE, cAMP-DEPENDENT, REGULATORY, TYPE I, ALPHA; PRKAR1A *188840 : TITIN; TTN *188850 : TL ANTIGEN *188855 : GRANULYSIN; GNLY *188860 : T-LYMPHOCYTE MATURATION-ASSOCIATED PROTEIN; MAL #188890 : TOBACCO ADDICTION 189000 : TOE, FIFTH, NUMBER OF PHALANGES IN 189100 : TOE, MISSHAPEN 189150 : TOE, ROTATED FIFTH 189200 : TOES, RELATIVE LENGTH OF FIRST AND SECOND 189230 : TOES, SPACE BETWEEN FIRST AND SECOND 189300 : TONGUE CURLING, FOLDING, OR ROLLING 189490 : TOOTH MALFORMATION #189500 : WITKOP SYNDROME 189600 : TORTICOLLIS *189700 : TORUS PALATINUS AND TORUS MANDIBULARIS *189800 : PREECLAMPSIA/ECLAMPSIA 1; PEE1 *189880 : TRANSFER RNA ASPARAGINE; TRN *189889 : TRANSCRIPTION FACTOR CP2; TFCP2 *189890 : TRANSFER RNA ASPARAGINE-LIKE; TRNL *189901 : TRANSCRIPTION FACTOR 9; TCF9 *189902 : TRANSCRIPTION FACTOR DP1; TFDP1 *189903 : NUCLEAR TRANSCRIPTION FACTOR Y, ALPHA; NFYA *189904 : NUCLEAR TRANSCRIPTION FACTOR Y, BETA; NFYB *189905 : TRANSCOBALAMIN I; TCN1 *189906 : TRANSCRIPTION FACTOR Sp1; SP1 *189907 : TRANSCRIPTION FACTOR 2; TCF2 *189908 : TRANSCRIPTION FACTOR 7; TCF7 *189909 : TRANSCRIPTION FACTOR 8; TCF8 *189910 : TRANSFER RNA SERINE 2; TRS2 *189911 : TRANSFER RNA GLYCINE-GCC-1; TRG1 *189912 : TRANSFER RNA PROLINE 3; TRP3 *189913 : TRANSFER RNA THREONINE 1; TRT1 *189918 : TRANSFER RNA LYSINE 1; TRK1 *189919 : TRANSFER RNA GLUTAMINE 1; TRQ1 *189920 : TRANSFER RNA LEUCINE 2; TRL2 *189921 : TRANSFER RNA CLUSTER 3; TRNP3 *189923 : TRANSFER RNA GLUTAMINE 2 *189930 : TRANSFER RNA PROLINE 1; TRP1 *189931 : TRANSFER RNA PROLINE 2; TRP2 *189932 : TRANSFER RNA LEUCINE 1 *189933 : TRANSFER RNA THREONINE 2; TRT2 *189940 : TRANSLOCATED PROMOTER REGION; TPR 189960 : TRACHEOESOPHAGEAL FISTULA WITH OR WITHOUT ESOPHAGEAL ATRESIA 189961 : TRACHEOPATHIA OSTEOPLASTICA *189962 : GENERAL TRANSCRIPTION FACTOR IIE, POLYPEPTIDE 1; GTF2E1 *189963 : GENERAL TRANSCRIPTION FACTOR IIB; GTF2B *189964 : GENERAL TRANSCRIPTION FACTOR IIE, POLYPEPTIDE 2; GTF2E2 *189965 : CCAAT/ENHANCER-BINDING PROTEIN, BETA; CEBPB *189967 : TEA DOMAIN FAMILY MEMBER 1; TEAD1 *189968 : GENERAL TRANSCRIPTION FACTOR IIF, POLYPEPTIDE 1, 74-KD; GTF2F1 *189969 : GENERAL TRANSCRIPTION FACTOR IIF, POLYPEPTIDE 2, 30-KD; GTF2F2 *189970 : GUANINE NUCLEOTIDE-BINDING PROTEIN, GAMMA-TRANSDUCING ACTIVITY POLYPEPTIDE 1; GNGT1 *189971 : E2F TRANSCRIPTION FACTOR 1; E2F1 *189972 : GENERAL TRANSCRIPTION FACTOR IIH, POLYPEPTIDE 1; GTF2H1 *189973 : TRANSCRIPTION FACTOR ELF 1; ELF1 189974 : TRANSDUCIN, BETA POLYPEPTIDE *189980 : ABELSON MURINE LEUKEMIA VIRAL ONCOGENE HOMOLOG 1; ABL1 *189990 : V-MYB AVIAN MYELOBLASTOSIS VIRAL ONCOGENE HOMOLOG; MYB *190000 : TRANSFERRIN; TF *190010 : TRANSFERRIN RECEPTOR; TFRC *190020 : V-HA-RAS HARVEY RAT SARCOMA VIRAL ONCOGENE HOMOLOG; HRAS *190030 : V-FES FELINE SARCOMA VIRAL/V-FPS FUJINAMI AVIAN SARCOMA VIRAL ONCOGENE HOMOLOG; FES *190040 : PLATELET-DERIVED GROWTH FACTOR, BETA POLYPEPTIDE; PDGFB *190060 : V-MOS MOLONEY MURINE SARCOMA VIRAL ONCOGENE HOMOLOG; MOS *190070 : V-KI-RAS2 KIRSTEN RAT SARCOMA 2 VIRAL ONCOGENE HOMOLOG; KRAS2 *190080 : V-MYC AVIAN MYELOCYTOMATOSIS VIRAL ONCOGENE HOMOLOG; MYC *190090 : V-SRC AVIAN SARCOMA (SCHMIDT-RUPPIN A-2) VIRAL ONCOGENE; SRC *190100 : GENIOSPASM 1; GSM1 ^190110 : MOVED TO 190070 *190120 : THYROID HORMONE RECEPTOR, ALPHA-1; THRA *190151 : V-ERB-B2 AVIAN ERYTHROBLASTIC LEUKEMIA VIRAL ONCOGENE HOMOLOG 3; ERBB3 *190160 : THYROID HORMONE RECEPTOR, BETA; THRB *190170 : TRANSFORMING GROWTH FACTOR, ALPHA; TGFA *190180 : TRANSFORMING GROWTH FACTOR, BETA-1; TGFB1 *190181 : TRANSFORMING GROWTH FACTOR-BETA RECEPTOR, TYPE I; TGFBR1 *190182 : TRANSFORMING GROWTH FACTOR-BETA RECEPTOR, TYPE II; TGFBR2 ^190190 : MOVED TO 154280 *190195 : TRANSGLUTAMINASE 1; TGM1 *190196 : TRANSGLUTAMINASE 2; TGM2 *190197 : CONTACTIN 2; CNTN2 *190198 : NOTCH, DROSOPHILA, HOMOLOG OF, 1; NOTCH1 190200 : TREMOR OF INTENTION, ATAXIA, AND LIPOFUSCINOSIS *190220 : TRANSFORMING GROWTH FACTOR, BETA-2; TGFB2 *190230 : TRANSFORMING GROWTH FACTOR, BETA-3; TGFB3 *190231 : TRANSITION PROTEIN 1; TNP1 *190232 : TRANSITION PROTEIN 2; TNP2 *190300 : TREMOR, HEREDITARY ESSENTIAL, 1; ETM1 *190310 : TREMOR, NYSTAGMUS, AND DUODENAL ULCER *190315 : SOLUTE CARRIER FAMILY 25, MEMBER 1; SLC25A1 #190320 : TRICHODENTOOSSEOUS SYNDROME 190330 : TRICHOMEGALY 190340 : TRICHODISCOMAS, FAMILIAL MULTIPLE 190345 : TRICHOEPITHELIOMAS, MULTIPLE DESMOPLASTIC #190350 : TRICHORHINOPHALANGEAL SYNDROME, TYPE I; TRPS1 #190351 : TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3 190360 : TRICHODYSPLASIA-XERODERMA *190370 : TRICHOHYALIN; THH 190400 : TRIGEMINAL NEURALGIA 190410 : TRIGGER THUMB 190420 : TRIGLYCERIDE STORAGE DISEASE, TYPE I 190430 : TRIGLYCERIDE STORAGE DISEASE, TYPE II 190440 : TRIGONOCEPHALY 190445 : TRIIODOTHYRONINE RECEPTOR AUXILIARY PROTEIN; TRAP *190450 : TRIOSEPHOSPHATE ISOMERASE 1; TPI1 *190470 : TRIPEPTIDYL PEPTIDASE II; TPP2 190500 : TRIPHALANGEAL THUMB WITH DOUBLE PHALANGES *190600 : TRIPHALANGEAL THUMB, NONOPPOSABLE *190605 : TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME 190650 : TRIPHALANGEAL THUMBS AND DISLOCATION OF PATELLA *190680 : TRIPHALANGEAL THUMBS WITH BRACHYECTRODACTYLY #190685 : DOWN SYNDROME *190700 : ZINC FINGER PROTEIN 36, MOUSE, HOMOLOG OF; ZFP36 190800 : TRISTICHIASIS *190900 : TRITANOPIA *190920 : TROPHOBLAST GLYCOPROTEIN; TPBG *190930 : TROPOMODULIN; TMOD *190940 : ENDOGENOUS RETROVIRAL SEQUENCE, TRUNCATED 1; ERVT1 *190950 : ENDOGENOUS RETROVIRAL SEQUENCE, TRUNCATED 2; ERVT2 *190960 : ENDOGENOUS RETROVIRAL SEQUENCE, TRUNCATED 3; ERVT3 *190970 : ENDOGENOUS RETROVIRAL SEQUENCE, TRUNCATED 4; ERVT4 *190980 : ENDOGENOUS RETROVIRAL SEQUENCE, TRUNCATED 5; ERVT5 *190990 : TROPOMYOSIN 2; TPM2 191000 : TROCHLEA OF THE HUMERUS, APLASIA OF *191010 : TROPOMYOSIN 1; TPM1 *191020 : TROPHOBLAST-LYMPHOCYTE CROSSREACTIVE ANTIGEN *191030 : TROPOMYOSIN 3; TPM3 *191039 : TROPONIN C, FAST; TNNC2 *191040 : TROPONIN C, SLOW; TNNC1 *191041 : TROPONIN T1, SKELETAL, SLOW; TNNT1 *191042 : TROPONIN I, SLOW-TWITCH SKELETAL MUSCLE ISOFORM; TNNI1 *191043 : TROPONIN I, FAST-TWITCH SKELETAL MUSCLE ISOFORM; TNNI2 *191044 : TROPONIN I, CARDIAC; TNNI3 *191045 : TROPONIN T2, CARDIAC; TNNT2 *191050 : TRYPTOPHANYL-tRNA SYNTHETASE; WARS *191060 : TRYPTOPHAN HYDROXYLASE; TPH *191070 : TRYPTOPHAN 2,3-DIOXYGENASE; TDO2 *191080 : TRYPTASE, ALPHA; TPS1 *191081 : TRYPTASE, BETA-1; TPSB1 191090 : TUBEROUS SCLEROSIS 4 191091 : TUBEROUS SCLEROSIS 3; TSC3 *191092 : TUBEROUS SCLEROSIS 2 GENE; TSC2 #191100 : TUBEROUS SCLEROSIS; TS *191110 : TUBULIN, ALPHA-1; TUBA1 *191120 : TUBULIN, ALPHA-LIKE 1; TUBAL1 *191130 : TUBULIN, BETA; TUBB *191135 : TUBULIN, GAMMA-1; TUBG1 191150 : TUFTSIN DEFICIENCY *191155 : TRANSMEMBRANE 4 SUPERFAMILY, MEMBER 1; TM4SF1 *191160 : TUMOR NECROSIS FACTOR; TNF *191161 : TUMOR NECROSIS FACTOR-ALPHA-INDUCED PROTEIN 1; TNFAIP1 *191163 : TUMOR NECROSIS FACTOR-ALPHA-INDUCED PROTEIN 3; TNFAIP3 *191164 : EPHRIN A1; EFNA1 *191170 : TUMOR PROTEIN p53; TP53 *191175 : TUMOR REJECTION ANTIGEN 1; TRA1 *191181 : SUPPRESSOR OF TUMORIGENICITY 3; ST3 *191190 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 1A; TNFRSF1A *191191 : TUMOR NECROSIS FACTOR RECEPTOR SUBFAMILY, MEMBER 1B; TNFRSF1B *191195 : TUMOR PROGRESSION LOCUS 2; TPL2 *191200 : TUNE DEAFNESS 191250 : TWINNING DUE TO SUPERFETATION 191270 : TYROSINASE-LIKE; TYRL *191275 : DOPACHROME TAUTOMERASE; DCT *191290 : TYROSINE HYDROXYLASE; TH *191305 : TYROSINE KINASE, B-LYMPHOCYTE SPECIFIC; BLK *191306 : KINASE INSERT DOMAIN RECEPTOR; KDR ^191309 : MOVED TO 190151 *191311 : DISCOIDIN DOMAIN RECEPTOR FAMILY, MEMBER 2; DDR2 *191315 : NEUROTROPHIC TYROSINE KINASE, RECEPTOR, TYPE 1; NTRK1 *191316 : NEUROTROPHIC TYROSINE KINASE, RECEPTOR, TYPE 3; NTRK3 *191317 : U2 SMALL NUCLEAR RNA AUXILIARY FACTOR 1; U2AF1 *191318 : U2 SMALL NUCLEAR RIBONUCLEOPROTEIN AUXILIARY FACTOR, 65-KD SUBUNIT; U2AF65 *191320 : UBIQUITIN *191321 : UBIQUITIN A-52-RESIDUE RIBOSOMAL PROTEIN FUSION PRODUCT; UBA52 *191325 : UBIQUITIN-ACTIVATING ENZYME E1-LIKE; UBE1L *191327 : UBIQUINOL-CYTOCHROME c REDUCTASE, RIESKE IRON-SULFUR; UQCRFS1 *191328 : UBIQUINOL-CYTOCHROME c REDUCTASE CORE PROTEIN I; UQCRC1 *191329 : UBIQUINOL-CYTOCHROME c REDUCTASE CORE PROTEIN II; UQCRC2 *191330 : UBIQUINOL-CYTOCHROME c REDUCTASE-BINDING PROTEIN; UQCRB *191339 : UBIQUITIN B; UBB *191340 : UBIQUITIN C; UBC *191342 : UBIQUITIN CARBOXYL-TERMINAL ESTERASE L1; UCHL1 *191343 : RIBOSOMAL PROTEIN S27a; RPS27A ^191344 : MOVED TO 191321 *191350 : UDP-GlcNAc:DOLICHYL-PHOSPHATE N-ACETYLGLUCOSAMINEPHOSPHOTRANSFERASE #191390 : ULCERATIVE COLITIS, SUSCEPTIBILITY TO 191400 : ULNA AND FIBULA, HYPOPLASIA OF 191420 : ULNA METAPHYSEAL DYSPLASIA SYNDROME 191440 : ULNAR HYPOPLASIA *191480 : UNCOMBABLE HAIR SYNDROME 191482 : UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, AND BRACHYDACTYLY *191500 : UNDRITZ ANOMALY *191510 : GENE UPSTREAM OF NRAS *191520 : UPINGTON DISEASE *191523 : UPSTREAM STIMULATORY FACTOR 1; USF1 *191525 : URACIL DNA GLYCOSYLASE; UNG *191530 : URATE-BINDING GLOBULIN, DECREASE IN *191540 : URATE OXIDASE; UOX *191550 : URETER, BIFID OR DOUBLE 191600 : URETER, CANCER OF 191650 : URETEROCELE 191700 : URIC ACID UROLITHIASIS *191710 : URIDINE MONOPHOSPHATE KINASE; UMPK *191720 : 5-PRIME,3-PRIME-@NUCLEOTIDASE, CYTOSOLIC; NT5C *191730 : URIDINE PHOSPHORYLASE; UP *191740 : UDP-GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A1; UGT1A1 ^191741 : MOVED TO 191740 ^191742 : MOVED TO 600067 AND 191740 ^191743 : MOVED TO 191742 *191750 : URIDYL DIPHOSPHATE GLUCOSE PYROPHOSPHORYLASE 1; UGP1 *191760 : URIDYL DIPHOSPHATE GLUCOSE PYROPHOSPHORYLASE 2; UGP2 191800 : URINARY BLADDER, ATONY OF ^191810 : MOVED TO 131530 *191830 : UROGENITAL ADYSPLASIA, HEREDITARY *191840 : PLASMINOGEN ACTIVATOR, UROKINASE; PLAU *191845 : UROMODULIN; UMOD 191850 : URTICARIA, AQUAGENIC #191900 : MUCKLE-WELLS SYNDROME 191950 : URTICARIA, FAMILIAL LOCALIZED HEAT 192000 : UTERINE ANOMALIES *192020 : UTEROGLOBIN; UGB 192050 : UTERUS BICORNIS BICOLLIS WITH PARTIAL VAGINAL SEPTUM AND UNILATERAL HEMATOCOLPOS WITH IPSILATERAL RENAL AGENESIS *192070 : UV-DAMAGE, EXCISION REPAIR OF, UV-24 *192090 : CADHERIN 1; CDH1 192100 : UVULA, BIFID *192130 : ATPase, H+ TRANSPORTING, LYSOSOMAL, NONCATALYTIC ACCESSORY PROTEIN 1A; ATP6N1A *192132 : ATPase, H+ TRANSPORTING, LYSOSOMAL 56/58-KD, V1 SUBUNIT B, ISOFORM 1; ATP6V1B1 *192150 : VALYL-tRNA SYNTHETASE 1; VARS1 192200 : VARICOSE VEINS *192225 : VASCULAR CELL ADHESION MOLECULE 1; VCAM1 *192240 : VASCULAR ENDOTHELIAL GROWTH FACTOR; VEGF 192300 : VASCULAR HELIX OF UMBILICAL CORD 192310 : VASCULITIS, HEREDITARY INFLAMMATORY, WITH PERSISTENT NODULES *192315 : VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY *192320 : VASOACTIVE INTESTINAL PEPTIDE; VIP *192321 : VASOACTIVE INTESTINAL PEPTIDE RECEPTOR 1; VIPR1 *192340 : ARGININE VASOPRESSIN; AVP 192350 : VATER ASSOCIATION 192400 : VEINS, PATTERN OF, ON ANTERIOR THORAX #192430 : VELOCARDIOFACIAL SYNDROME 192445 : VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE ^192450 : MOVED TO 603829 *192500 : LONG QT SYNDROME 1 #192600 : CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC; CMH #192605 : VENTRICULAR TACHYCARDIA, FAMILIAL 192700 : VENULAR INSUFFICIENCY, SYSTEMIC 192800 : VERTEBRAL FUSION, POSTERIOR LUMBOSACRAL, WITH BLEPHAROPTOSIS *192900 : VERTEBRAL HYPOPLASIA WITH LUMBAR KYPHOSIS 192950 : VERTICAL TALUS, CONGENITAL; CVT *192968 : INTEGRIN, ALPHA-1; ITGA1 ^192972 : MOVED TO 192975 *192974 : INTEGRIN, ALPHA-2; ITGA2 *192975 : INTEGRIN, ALPHA-4; ITGA4 *192977 : VERY LOW DENSITY LIPOPROTEIN RECEPTOR; VLDLR *193000 : VESICOURETERAL REFLUX; VUR *193001 : SOLUTE CARRIER FAMILY 18, MEMBER 2; SLC18A2 *193002 : SOLUTE CARRIER FAMILY 18, MEMBER 1; SLC18A1 193003 : VESTIBULOCEREBELLAR DISORDER WITH PREDOMINANT OCULAR SIGNS 193005 : VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE 193007 : VESTIBULOPATHY, FAMILIAL ^193010 : MOVED TO 112266 *193040 : VILLIN; VIL 193050 : VIBRATORY ANGIOEDEMA *193060 : VIMENTIN; VIM *193065 : VINCULIN; VCL *193067 : FRIEND LEUKEMIA VIRUS INTEGRATION 1; FLI1 193070 : VIRUS RD114 RNA COMPLEMENTARITY *193090 : R BINDER PROTEIN #193100 : HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT; ADHR *193190 : VITRONECTIN; VTN *193200 : VITILIGO *193210 : INTEGRIN, ALPHA-V; ITGAV *193220 : VITREORETINOCHOROIDOPATHY; VRCP 193230 : VITREORETINAL DEGENERATION, SNOWFLAKE TYPE *193235 : VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY; VRNI 193240 : VOCAL CORD PARALYSIS AND PTOSIS *193245 : VOLTAGE-DEPENDENT ANION CHANNEL 2; VDAC2 *193250 : VOLVULUS OF MIDGUT ^193290 : MOVED TO 151675 *193300 : VON HIPPEL-LINDAU SYNDROME; VHL *193400 : VON WILLEBRAND DISEASE 193450 : VULVOVAGINITIS, ALLERGIC SEMINAL #193500 : WAARDENBURG SYNDROME, TYPE I; WS1 #193510 : WAARDENBURG SYNDROME, TYPE IIA; WS2A #193520 : WATSON SYNDROME *193525 : WEE 1 TYROSINE KINASE; WEE1 #193530 : WEYERS ACROFACIAL DYSOSTOSIS *193670 : WHIM SYNDROME ^193675 : REMOVED FROM DATABASE 193680 : WHISPERING DYSPHONIA, HEREDITARY *193700 : WHISTLING FACE-WINDMILL VANE HAND SYNDROME #193900 : WHITE SPONGE NEVUS OF CANNON 194000 : WIDOW'S PEAK #194050 : WILLIAMS-BEUREN SYNDROME; WBS *194070 : WILMS TUMOR 1; WT1 *194071 : MULTIPLE TUMOR-ASSOCIATED CHROMOSOME REGION 1; MTACR1 #194072 : WAGR SYNDROME #194080 : WILMS TUMOR AND PSEUDOHERMAPHRODITISM *194090 : WILMS TUMOR 3; WT3 194100 : WISDOM TEETH, ABSENCE OF #194190 : WOLF-HIRSCHHORN SYNDROME; WHS #194200 : WOLFF-PARKINSON-WHITE SYNDROME *194300 : WOOLLY HAIR, AUTOSOMAL DOMINANT 194320 : WORONETS TRAIT *194350 : WT LIMB-BLOOD SYNDROME *194355 : X BOX-BINDING PROTEIN 1; XBP1 *194360 : X-RAY REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 1; XRCC1 *194363 : X-RAY REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 4; XRCC4 *194364 : X-RAY REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 5; XRCC5 194370 : X-RAY SENSITIVITY; XRS *194380 : DEHYDRATED HEREDITARY STOMATOCYTOSIS; DHS 194400 : XERODERMA PIGMENTOSUM, AUTOSOMAL DOMINANT, MILD *194450 : YEAST FACTOR *194460 : ZINC-ALPHA-2-GLYCOPROTEIN; AZGP1; ZAG; ZA2G *194470 : ZINC, ELEVATED PLASMA *194480 : ZINC FINGER PROTEIN 3, MOUSE, HOMOLOG OF; ZFP3 *194490 : ZINC FINGER PROTEIN 1; ZNF1 *194500 : ZINC FINGER PROTEIN 2; ZNF2 *194510 : ZINC FINGER PROTEIN 3; ZNF3 *194520 : ZINC FINGER PROTEIN 4; ZNF4 *194521 : ZINC FINGER PROTEIN 11A; ZNF11A 194522 : ZINC FINGER PROTEIN 11B; ZNF11B *194524 : ZINC FINGER PROTEIN 18; ZNF18 *194525 : ZINC FINGER PROTEIN 19; ZNF19 *194526 : ZINC FINGER PROTEIN 34; ZNF34 *194527 : ZINC FINGER PROTEIN 23; ZNF23 *194528 : ZINC FINGER PROTEIN 25; ZNF25 *194529 : ZINC FINGER PROTEIN 22; ZNF22 *194530 : ZINC FINGER PROTEIN 5; ZNF5 *194531 : ZINC FINGER PROTEIN 7; ZNF7 *194532 : ZINC FINGER PROTEIN 8; ZNF8 *194533 : ZINC FINGER PROTEIN 35; ZNF35 *194534 : ZINC FINGER PROTEIN 24; ZNF24 *194535 : ZINC FINGER PROTEIN 29; ZNF29 *194536 : ZINC FINGER PROTEIN 12; ZNF12 *194537 : ZINC FINGER PROTEIN 26; ZNF26 *194538 : ZINC FINGER PROTEIN 10; ZNF10 *194539 : ZINC FINGER PROTEIN 32; ZNF32 *194540 : HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 ENHANCER-BINDING PROTEIN 1; HIVEP1 *194541 : ZINC FINGER PROTEIN 46; ZNF46 *194542 : ZINC FINGER PROTEIN 44; ZNF44 *194543 : ZINC FINGER PROTEIN 69; ZNF69 *194544 : ZINC FINGER PROTEIN 70; ZNF70 *194545 : ZINC FINGER PROTEIN 71; ZNF71 *194546 : ZINC FINGER PROTEIN 72; ZNF72 *194547 : ZINC FINGER PROTEIN 73; ZNF73 *194548 : ZINC FINGER PROTEIN 74; ZNF74 *194549 : ZINC FINGER PROTEIN 76; ZNF76 *194550 : ZINC FINGER PROTEIN 42; ZNF42 *194551 : ZINC FINGER PROTEIN 77; ZNF77 *194552 : ZINC FINGER PROTEIN 79; ZNF79 *194553 : ZINC FINGER PROTEIN 80; ZNF80 *194554 : ZINC FINGER PROTEIN 13; ZNF13 *194555 : ZINC FINGER PROTEIN 27; ZNF27 *194556 : ZINC FINGER PROTEIN 14; ZNF14 *194557 : ZINC FINGER PROTEIN 20; ZNF20 *194558 : ZINC FINGER PROTEIN 83; ZNF83 *194624 : ZINC FINGER PROTEIN 117; ZNF117 *194628 : ZINC FINGER PROTEIN 121; ZNF121 *194630 : ZINC FINGER PROTEIN 123; ZNF123 *194631 : ZINC FINGER PROTEIN 124; ZNF124 *194632 : ZINC FINGER PROTEIN 125; ZNF125 *194633 : ZINC FINGER PROTEIN 126; ZNF126 *194648 : ZINC FINGER PROTEIN 141; ZNF141 *195000 : ZONA PELLUCIDA GLYCOPROTEIN 1; ZP1 *195002 : ZONA PELLUCIDA GLYCOPROTEIN 3B; ZP3B #200100 : ABETALIPOPROTEINEMIA; ABL 200110 : ABLEPHARON-MACROSTOMIA SYNDROME 200130 : ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION #200150 : CHOREOACANTHOCYTOSIS; CHAC 200170 : ACANTHOSIS NIGRICANS WITH MUSCLE CRAMPS AND ACRAL ENLARGEMENT 200300 : ACETOPHENETIDIN SENSITIVITY *200350 : ACETYL-CoA CARBOXYLASE DEFICIENCY *200400 : ACHALASIA, FAMILIAL ESOPHAGEAL 200440 : ACHALASIA-ALACRIMA SYNDROME 200450 : ACHALASIA-MICROCEPHALY SYNDROME #200500 : ACHEIROPODY *200600 : ACHONDROGENESIS, TYPE IA; ACG1A #200610 : ACHONDROGENESIS, TYPE II; ACG2 #200700 : CHONDRODYSPLASIA, GREBE TYPE 200710 : ACHONDROGENESIS, TYPE III 200720 : ACHONDROGENESIS, TYPE IV 200900 : ACHONDROPLASIA, SO-CALLED, AND SWISS-TYPE AGAMMAGLOBULINEMIA ^200930 : REMOVED FROM DATABASE #200950 : ACID PHOSPHATASE DEFICIENCY 200970 : ACKERMAN SYNDROME 200980 : ACRORENAL-MANDIBULAR SYNDROME *200990 : ACROCALLOSAL SYNDROME; ACLS 200995 : ACROCEPHALOPOLYDACTYLOUS DYSPLASIA *201000 : ACROCEPHALOPOLYSYNDACTYLY TYPE II 201020 : ACROCEPHALOPOLYSYNDACTYLY TYPE IV 201050 : ACROCRANIOFACIAL DYSOSTOSIS #201100 : ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE; AEZ 201170 : ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ 201180 : ACROFRONTOFACIONASAL DYSOSTOSIS SYNDROME ^201181 : MOVED TO 239710 201200 : ACROGERIA, GOTTRON TYPE #201250 : ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE *201300 : ACROOSTEOLYSIS, NEUROGENIC 201310 : ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE #201400 : ACTH DEFICIENCY #201450 : ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF *201460 : ACYL-CoA DEHYDROGENASE, LONG-CHAIN, DEFICIENCY OF #201470 : ACYL-CoA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF *201475 : ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF *201550 : ADDUCTED THUMBS SYNDROME #201710 : LIPOID CONGENITAL ADRENAL HYPERPLASIA 201750 : ADRENAL HYPERPLASIA, CONGENITAL, DUE TO DEFECTS IN SEVERAL STEROID-BIOSYNTHETIC ENZYMES *201810 : ADRENAL HYPERPLASIA II *201910 : ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY *202010 : ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 11-BETA-HYDROXYLASE DEFICIENCY *202110 : ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY 202150 : ADRENAL HYPOPLASIA, CONGENITAL, WITH ABSENT PITUITARY LUTEINIZING HORMONE 202155 : ADRENAL HYPOPLASIA, CYTOMEGALIC TYPE *202200 : ADRENAL UNRESPONSIVENESS TO ACTH #202300 : ADRENOCORTICAL CARCINOMA, HEREDITARY; ADCC 202355 : ADRENOCORTICAL UNRESPONSIVENESS TO ACTH WITH POSTRECEPTOR DEFECT #202370 : ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM #202400 : AFIBRINOGENEMIA, CONGENITAL *202500 : SEVERE COMBINED IMMUNODEFICIENCY 1; SCID1 202550 : AGANGLIONOSIS, TOTAL INTESTINAL 202600 : AGENESIS OF CEREBRAL WHITE MATTER *202650 : DYSGNATHIA COMPLEX 202660 : AGONADISM WITH MULTIPLE INTERNAL MALFORMATIONS #202700 : NEUTROPENIA, CONGENITAL, AUTOSOMAL DOMINANT OR SPORADIC 202900 : ALANINURIA WITH MICROCEPHALY, DWARFISM, ENAMEL HYPOPLASIA, AND DIABETES MELLITUS 203000 : FRONTONASAL DYSPLASIA WITH ALAR CLEFTS #203100 : OCULOCUTANEOUS ALBINISM, TYPE I; OCA1 *203200 : OCULOCUTANEOUS ALBINISM, TYPE II; OCA2 203280 : ALBINISM, MINIMAL PIGMENT TYPE 203285 : ALBINISM WITH IMMUNE AND HEMATOLOGIC DEFECTS #203290 : OCULOCUTANEOUS ALBINISM, TYPE III; OCA3 #203300 : HERMANSKY-PUDLAK SYNDROME; HPS #203310 : ALBINISM, OCULAR, AUTOSOMAL RECESSIVE; OAR 203330 : ALBRIGHT HEREDITARY OSTEODYSTROPHY; AHO 203340 : ALBINISM-MICROCEPHALY-DIGITAL ANOMALIES SYNDROME #203400 : ALDOSTERONE DEFICIENCY DUE TO DEFECT IN 18-HYDROXYLASE #203450 : ALEXANDER DISEASE *203500 : ALKAPTONURIA 203550 : ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME 203600 : ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN *203650 : ALOPECIA-MENTAL RETARDATION SYNDROME #203655 : ALOPECIA UNIVERSALIS CONGENITA; ALUNC *203700 : ALPERS DIFFUSE DEGENERATION OF CEREBRAL GRAY MATTER WITH HEPATIC CIRRHOSIS *203740 : ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY *203750 : ALPHA-METHYLACETOACETICACIDURIA 203760 : ALPHA-2-DEFICIENT COLLAGEN DISEASE #203780 : ALPORT SYNDROME, AUTOSOMAL RECESSIVE #203800 : ALSTROM SYNDROME; ALMS #204000 : LEBER CONGENITAL AMAUROSIS, TYPE I; LCA1 #204100 : LEBER CONGENITAL AMAUROSIS, TYPE II; LCA2 204110 : AMAUROSIS CONGENITA, CONE-ROD TYPE, WITH CONGENITAL HYPERTRICHOSIS #204200 : CEROID LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3 *204300 : CEROID LIPOFUSCINOSIS, NEURONAL 4; CLN4 ^204400 : REMOVED FROM DATABASE *204500 : CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 *204600 : AMAUROTIC IDIOCY, LATE INFANTILE TYPE, WITH MULTILAMELLAR CYTOSOMES 204650 : AMELOGENESIS IMPERFECTA, LOCAL HYPOPLASTIC TYPE, RECESSIVE 204690 : AMELOGENESIS IMPERFECTA AND NEPHROCALCINOSIS *204700 : AMELOGENESIS IMPERFECTA, PIGMENTED HYPOMATURATION TYPE 204730 : AMINOACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY, OSTEOPOROSIS, AND ACIDOSIS 204750 : AMINOADIPICACIDURIA *204800 : AMOBARBITAL, DEFICIENT N-HYDROXYLATION OF 204850 : AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION #204870 : CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE 204900 : AMYLOIDOSIS, CUTANEOUS BULLOUS #205000 : AMYOTONIA CONGENITA #205100 : AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2 *205200 : AMYOTROPHIC LATERAL SCLEROSIS, JUVENILE, WITH DEMENTIA 205250 : AMYOTROPHIC LATERAL SCLEROSIS WITH POLYGLUCOSAN BODIES #205400 : TANGIER DISEASE; TGD 205600 : ANEMIA AND TRIPHALANGEAL THUMBS 205700 : ANEMIA, AUTOIMMUNE HEMOLYTIC #205900 : DIAMOND-BLACKFAN ANEMIA; DBA 205950 : ANEMIA, CONGENITAL SIDEROBLASTIC, B6-NONRESPONSIVE 206000 : ANEMIA, FAMILIAL PYRIDOXINE-RESPONSIVE 206100 : ANEMIA, HYPOCHROMIC MICROCYTIC 206200 : ANEMIA, MICROCYTIC 206300 : ANEMIA, NONSPHEROCYTIC HEMOLYTIC, ASSOCIATED WITH ABNORMALITY OF RED CELL MEMBRANE 206400 : ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRIN METABOLISM *206500 : ANENCEPHALY 206550 : ANGIOLIPOMATOSIS, FAMILIAL *206570 : ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT 206600 : ANHIDROSIS *206700 : ANIRIDIA, CEREBELLAR ATAXIA, AND MENTAL DEFICIENCY 206750 : ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTOR RETARDATION *206780 : ANODONTIA, COMPLETE, OF PERMANENT DENTITION *206800 : ANONYCHIA *206900 : ANOPHTHALMOS, TRUE OR PRIMARY *206920 : ANOPHTHALMOS WITH LIMB ANOMALIES 207000 : ANOSMIA FOR ISOBUTYRIC ACID 207300 : ANTITHROMBIN, FAMILIAL HEMORRHAGIC DIATHESIS DUE TO *207410 : ANTLEY-BIXLER SYNDROME; ABS 207500 : ANUS, IMPERFORATE 207600 : TAKAYASU ARTERITIS 207620 : APHALANGY WITH HEMIVERTEBRAE 207700 : APLASIA CUTIS CONGENITA; ACC 207720 : APNEA, CENTRAL SLEEP 207731 : APLASIA CUTIS CONGENITA WITH INTESTINAL LYMPHANGIECTASIA 207740 : APLASIA OF EXTENSOR MUSCLES OF FINGERS, UNILATERAL, WITH GENERALIZED POLYNEUROPATHY *207750 : APOLIPOPROTEIN C-II DEFICIENCY, TYPE I HYPERLIPOPROTEINEMIA DUE TO 207765 : APPARENT MINERALOCORTICOID EXCESS, TYPE 2; AME2 207770 : APROSENCEPHALY SYNDROME 207780 : AREDYLD 207790 : ARACHNOID CYSTS, INTRACRANIAL *207800 : ARGININEMIA *207900 : ARGININOSUCCINICACIDURIA 207950 : ARNOLD-CHIARI MALFORMATION *208000 : ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY 208050 : ARTERIAL TORTUOSITY *208060 : ARTERIOSCLEROSIS, SEVERE JUVENILE 208080 : ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION, AND FACIAL ANOMALIES 208081 : ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTIC FACIES 208085 : ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS *208100 : ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE; AMCN ^208110 : MOVED TO 208155 *208150 : PENA-SHOKEIR SYNDROME, TYPE I 208155 : ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE 208158 : ARTHROGRYPOSIS WITH HYPERKERATOSIS *208200 : ARTHROGRYPOSIS-LIKE DISORDER #208230 : ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD; PPAC #208250 : ARTHROPATHY-CAMPTODACTYLY SYNDROME 208300 : ASCITES, CHYLOUS *208400 : ASPARTYLGLUCOSAMINURIA *208500 : ASPHYXIATING THORACIC DYSTROPHY; ATD 208530 : ASPLENIA WITH CARDIOVASCULAR ANOMALIES 208540 : ASPLENIA WITH CYSTIC LIVER, KIDNEY AND PANCREAS 208550 : ASTHMA, NASAL POLYPS, ASPIRIN INTOLERANCE 208600 : ASTHMA, SHORT STATURE, AND ELEVATED IgA 208700 : ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA *208750 : ATAXIA, DEAFNESS, AND CARDIOMYOPATHY *208800 : PYRUVATE DECARBOXYLASE DEFICIENCY 208850 : ATAXIA-DEAFNESS-RETARDATION SYNDROME 208870 : ATAXIA-MICROCEPHALY-CATARACT SYNDROME *208900 : ATAXIA-TELANGIECTASIA; AT ^208905 : MOVED TO 208900 208910 : ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH #208920 : ATAXIA-OCULOMOTOR APRAXIA SYNDROME 209000 : ATAXIC DIPLEGIA WITH DEFECTIVE CELLULAR IMMUNITY 209010 : ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS, PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE 209050 : ATHROMBIA, ESSENTIAL *209100 : ATONIC-ASTATIC SYNDROME OF FOERSTER #209300 : ATRANSFERRINEMIA ^209400 : MOVED TO 600309 #209500 : ATRICHIA WITH PAPULAR LESIONS; APL 209600 : ATRIOVENTRICULAR DISSOCIATION 209700 : ATROPHODERMIA VERMICULATA ^209750 : MOVED TO 209950 209770 : AURAL ATRESIA, MULTIPLE CONGENITAL ANOMALIES, AND MENTAL RETARDATION 209800 : AUSTRALIA ANTIGEN *209850 : AUTISM, SUSCEPTIBILITY TO, 1; AUTS1 #209880 : AUTONOMIC CONTROL, CONGENITAL FAILURE OF 209885 : BARBER-SAY SYNDROME #209900 : BARDET-BIEDL SYNDROME; BBS *209901 : BBS1 GENE; BBS1 #209920 : BARE LYMPHOCYTE SYNDROME, TYPE II ^209930 : MOVED TO 241200 #209950 : ATYPICAL MYCOBACTERIOSIS, FAMILIAL 209970 : BEEMER LETHAL MALFORMATION SYNDROME 210000 : BEHR SYNDROME 210050 : BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION *210100 : BETA-AMINOISOBUTYRIC ACID, URINARY EXCRETION OF *210200 : 3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY *210210 : 3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY #210250 : SITOSTEROLEMIA 210300 : BIEMOND CONGENITAL AND FAMILIAL ANALGESIA 210350 : BIEMOND SYNDROME II *210370 : BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY 210400 : BIFID NOSE 210450 : BILE ACID, SYNTHETIC DEFECT OF 210500 : BILIARY ATRESIA, EXTRAHEPATIC; EHBA 210550 : BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY *210600 : SECKEL SYNDROME 210700 : BIRD-HEADED DWARFISM, MONTREAL TYPE *210710 : MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I *210720 : MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II *210730 : MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III 210740 : BIRD-HEADED DWARFISM WITH PROGRESSIVE ATAXIA, INSULIN-RESISTANT DIABETES, GOITER, AND PRIMARY GONADAL INSUFFICIENCY 210745 : BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE 210750 : BLOND HAIR #210900 : BLOOM SYNDROME; BLM 211000 : BLUE DIAPER SYNDROME *211100 : FUCOSYLTRANSFERASE 1; FUT1 211120 : BONE DYSPLASIA, LETHAL, HOLMGREN TYPE 211170 : BORRONE DERMATOCARDIOSKELETAL SYNDROME *211180 : BOWEN HUTTERITE SYNDROME 211200 : BOWEN SYNDROME OF MULTIPLE MALFORMATIONS *211350 : KYPHOMELIC DYSPLASIA 211355 : BOWING OF LONG BONES, ASYMMETRIC AND SYMMETRIC 211369 : BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY 211370 : BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM 211380 : BRACHIOSKELETOGENITAL SYNDROME *211390 : BRITTLE HAIR AND MENTAL DEFICIT 211400 : BRONCHIECTASIS *211410 : BREAST CANCER, DUCTAL, 1; BRCD1 *211420 : BREAST CANCER, DUCTAL, 2; BRCD2 211450 : BRONCHOMALACIA 211480 : BUERGER DISEASE *211500 : BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD *211530 : BULBAR PALSY, PROGRESSIVE, WITH SENSORINEURAL DEAFNESS ^211550 : MOVED TO 113900 #211600 : CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1; PFIC1 *211750 : C SYNDROME 211770 : CAHMR SYNDROME 211800 : CALCIFICATION OF JOINTS AND ARTERIES *211890 : CAMPOMELIA, CUMMING TYPE *211900 : CALCINOSIS, TUMORAL, WITH HYPERPHOSPHATEMIA 211910 : CAMPTODACTYLY SYNDROME, GUADALAJARA TYPE I; GCS1 211920 : CAMPTODACTYLY SYNDROME, GUADALAJARA TYPE II 211930 : CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA *211960 : CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMAL PALMAR CREASES 211965 : CAMPTODACTYLY-ICHTHYOSIS SYNDROME ^211970 : MOVED TO 114290 #211980 : LUNG CANCER 211990 : CAMPTOMELIC SYNDROME, LONG-LIMB TYPE *212050 : CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE 212060 : CARBIMAZOLE SENSITIVITY #212065 : CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia #212066 : CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa 212067 : CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIx #212070 : CARBOXYPEPTIDASE N DEFICIENCY 212080 : CARDIAC LIPIDOSIS, FAMILIAL 212090 : CARDIAC SEPTAL DEFECTS WITH COARCTATION OF THE AORTA 212093 : CARDIAC VALVULAR DEFECT, DEVELOPMENTAL 212100 : CARDIOAUDITORY SYNDROME OF SANCHEZ CASCOS 212110 : CARDIOMYOPATHY, DILATED, AUTOSOMAL RECESSIVE 212112 : CARDIOMYOPATHY, CONGESTIVE, WITH HYPERGONADOTROPIC HYPOGONADISM 212120 : CARDIOGENITAL SYNDROME *212130 : CARDIOMYOPATHY ASSOCIATED WITH MYOPATHY AND SUDDEN DEATH 212135 : CARDIOSKELETAL SYNDROME, KUWAITI TYPE *212138 : SOLUTE CARRIER FAMILY 25 (CARNITINE/ACYLCARNITINE TRANSLOCASE), MEMBER 20; SLC25A20 #212140 : CARNITINE DEFICIENCY, SYSTEMIC PRIMARY; CDSP *212160 : CARNITINE DEFICIENCY, MYOPATHIC *212200 : CARNOSINEMIA *212350 : CATARACT AND CARDIOMYOPATHY 212360 : CATARACT-ALOPECIA-SCLERODACTYLY SYNDROME; CASS *212400 : CATARACT AND CONGENITAL ICHTHYOSIS *212500 : CATARACT, CONGENITAL OR JUVENILE 212540 : CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME 212550 : CATARACT, MICROPHTHALMIA, AND NYSTAGMUS ^212600 : REMOVED FROM DATABASE ^212700 : REMOVED FROM DATABASE 212710 : CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME 212720 : CATARACT-MENTAL RETARDATION-HYPOGONADISM *212750 : CELIAC DISEASE; CD *212780 : CENANI SYNDACTYLISM 212790 : PREMATURE CENTROMERE DIVISION 212800 : CEPHALIN LIPIDOSIS 212835 : CEREBELLAR ATAXIA AND ECTODERMAL DYSPLASIA *212840 : CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM 212850 : CEREBELLAR ATAXIA AND NEUROSENSORY DEAFNESS 212890 : CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA *212895 : CEREBELLAR ATAXIA, EARLY-ONSET, WITH RETAINED TENDON REFLEXES; EOCA 212900 : CEREBELLAR ATAXIA, INFANTILE, WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA 212905 : CEREBELLAR ATAXIA WITH NEURONAL MIGRATION DEFECT *213000 : CEREBELLAR HYPOPLASIA 213002 : CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS 213010 : CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZ SYNDROME AND MECKEL SYNDROME *213100 : CEREBELLOPARENCHYMAL DISORDER II; CPD II *213200 : CEREBELLAR ATAXIA 1; CLA1 *213300 : JOUBERT SYNDROME 1; JBTS1 213400 : CEREBELLOPARENCHYMAL DISORDER V; CPD V 213500 : CEREBRAL ANGIOPATHY, DYSPHORIC *213600 : FAHR DISEASE #213700 : CEREBROTENDINOUS XANTHOMATOSIS 213820 : CEREBRAL MALFORMATION, SEIZURES, HYPERTRICHOSIS, AND OVERLAPPING FINGERS 213900 : CEREBRAL SCLEROSIS SIMILAR TO PELIZAEUS-MERZBACHER DISEASE 213950 : CEREBROCORTICAL DEGENERATION OF INFANCY *213980 : CEREBROFACIOTHORACIC DYSPLASIA #214100 : ZELLWEGER SYNDROME; ZS *214110 : CEREBROHEPATORENAL SYNDROME, VARIANT TYPES #214150 : CEREBROOCULOFACIOSKELETAL SYNDROME 214200 : CEROID STORAGE DISEASE 214290 : CERVICAL VERTEBRAE, AGENESIS OF 214300 : CERVICAL VERTEBRAL FUSION, AUTOSOMAL RECESSIVE 214350 : CHANDS *214370 : NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, MENTAL RETARDATION, AND ABSENT SENSORY LARGE MYELINATED FIBERS 214380 : CHARCOT-MARIE-TOOTH DISEASE, PROGRESSIVE ATAXIA, AND TREMOR #214400 : CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A #214450 : GRISCELLI SYNDROME #214500 : CHEDIAK-HIGASHI SYNDROME; CHS #214700 : CHLORIDE DIARRHEA, FAMILIAL; CLD 214800 : CHOANAL ATRESIA, POSTERIOR; PCA *214900 : CHOLESTASIS-LYMPHEDEMA SYNDROME *214950 : CHOLESTASIS, INTRAHEPATIC, WITH DEFECTIVE METABOLISM OF TRIHYDROXYCOPROSTANIC ACID TO CHOLIC ACID 214980 : CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE 215030 : CHOLESTEROL PNEUMONIA #215045 : CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD 215050 : CHONDRODYSPLASIA CALCIFICANS METAPHYSEALIS #215100 : RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1 215105 : CHONDRODYSPLASIA PUNCTATA SYNDROME 215140 : CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE #215150 : OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED 215250 : CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME #215300 : CHONDROSARCOMA *215400 : CHORDOMA; CHDM 215450 : CHOREA, FAMILIAL BENIGN *215470 : CHORIORETINAL DYSTROPHY, SPINOCEREBELLAR ATAXIA, AND HYPOGONADOTROPIC HYPOGONADISM 215480 : CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION *215500 : CHOROIDAL DYSTROPHY, CENTRAL AREOLAR; CACD 215510 : CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY 215518 : CILIARY DISCOORDINATION DUE TO RANDOM CILIARY ORIENTATION *215520 : CILIARY DYSKINESIA DUE TO TRANSPOSITION OF CILIARY MICROTUBULES 215550 : CIRCUMVALLATE PLACENTA SYNDROME 215600 : CIRRHOSIS, FAMILIAL #215700 : CITRULLINEMIA, CLASSIC 215720 : CITRULLINE TRANSPORT DEFECT 215800 : CLEFT LARYNX, POSTERIOR 215850 : CLEFT-LIMB-HEART MALFORMATION SYNDROME 216100 : CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY 216300 : CLEFT PALATE, DEAFNESS, AND OLIGODONTIA 216330 : CLEIDOCRANIAL DYSPLASIA, RECESSIVE FORM *216340 : CLEIDOCRANIAL DYSPLASIA WITH MICROGNATHIA, ABSENT THUMBS, AND DISTAL APHALANGIA 216360 : COACH SYNDROME *216400 : COCKAYNE SYNDROME, TYPE I; CKN1 216411 : COCKAYNE SYNDROME, TYPE III *216550 : COHEN SYNDROME; COH1 *216700 : COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING 216800 : COLOBOMA OF MACULA AND SKELETAL ANOMALIES 216820 : COLOBOMA, OCULAR #216900 : ACHROMATOPSIA 2; ACHM2 216920 : COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT *216950 : COMPLEMENT COMPONENT C1r DEFICIENCY *217000 : COMPLEMENT COMPONENT 2 DEFICIENCY *217030 : I FACTOR; IF *217050 : COMPLEMENT COMPONENT 6 DEFICIENCY *217070 : COMPLEMENT COMPONENT 7 DEFICIENCY 217080 : CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA 217085 : CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY #217090 : CONJUNCTIVITIS, LIGNEOUS #217095 : CONOTRUNCAL HEART MALFORMATIONS; CTHM 217100 : CONSTRICTING BANDS, CONGENITAL 217150 : CONTRACTURES, CONGENITAL, TORTICOLLIS, AND MALIGNANT HYPERTHERMIA 217200 : CONVULSIVE DISORDER, FAMILIAL, WITH PRENATAL OR EARLY ONSET #217300 : CORNEA PLANA 2; CNA2 *217400 : CORNEAL DYSTROPHY AND SENSORINEURAL DEAFNESS *217500 : CORNEAL DYSTROPHY, BAND-SHAPED 217520 : CORNEAL DEGENERATION, BAND-SHAPED SPHEROID 217600 : CORNEAL DYSTROPHY, CENTRAL TYPE *217700 : CORNEAL ENDOTHELIAL DYSTROPHY 2; CHED2 #217800 : MACULAR DYSTROPHY, CORNEAL, 1; MCDC1 217980 : CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE 217990 : CORPUS CALLOSUM, AGENESIS OF *218000 : CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY 218010 : CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY *218030 : CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY *218040 : COSTELLO SYNDROME 218050 : CRAMPS, FAMILIAL ADOLESCENT 218090 : CRANE-HEISE SYNDROME *218100 : CRANIAL NERVES, CONGENITAL PARESIS OF 218200 : CRANIAL NERVES, RECURRENT PARESIS OF 218300 : CRANIODIAPHYSEAL DYSPLASIA; CDD *218330 : CRANIOECTODERMAL DYSPLASIA 218340 : CRANIOFACIAL DYSMORPHISM WITH OCULAR COLOBOMA, ABSENT CORPUS CALLOSUM, AND AORTIC DILATATION 218350 : CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE *218400 : CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR 218450 : CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS 218455 : CRANIOSYNOSTOSIS-MICROCEPHALY WITH CHROMOSOMAL BREAKAGE AND OTHER ABNORMALITIES 218500 : CRANIOSYNOSTOSIS 218530 : CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS 218550 : CRANIOSYNOSTOSIS WITH FIBULAR APLASIA 218600 : CRANIOSYNOSTOSIS WITH RADIAL DEFECTS 218649 : CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG 218650 : CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME 218670 : CRANIOTELENCEPHALIC DYSPLASIA #218700 : THYROID DYSGENESIS #218800 : CRIGLER-NAJJAR SYNDROME *218900 : CROME SYNDROME *219000 : FRASER SYNDROME 219050 : CRYPTORCHIDISM, UNILATERAL OR BILATERAL 219070 : CURVED NAIL OF FOURTH TOE 219080 : CUSHING DISEASE, ADRENAL 219090 : CUSHING DISEASE, PITUITARY 219095 : CUTANEOUS PHOTOSENSITIVITY AND COLITIS, LETHAL *219100 : CUTIS LAXA *219150 : CUTIS LAXA, CORNEAL CLOUDING, AND MENTAL RETARDATION #219200 : CUTIS LAXA WITH GROWTH AND DEVELOPMENTAL DELAY 219250 : CUTIS MARMORATA TELANGIECTATICA CONGENITA; CMTC 219300 : CUTIS VERTICIS GYRATA AND MENTAL DEFICIENCY; CVG/MR 219400 : CYANOSIS AND HEPATIC DISEASE *219500 : CYSTATHIONINURIA 219550 : CYSTEINE PEPTIDURIA 219600 : CYSTIC DISEASE OF LUNG #219700 : CYSTIC FIBROSIS; CF 219721 : CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND SUBNORMAL MENTALITY 219730 : CYSTIC KIDNEY DISEASE WITH VENTRICULOMEGALY #219750 : CYSTINOSIS, ADULT NONNEPHROPATHIC #219800 : CYSTINOSIS, NEPHROPATHIC; CTNS #219900 : CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE #220100 : CYSTINURIA; CSNU #220110 : COMPLEX IV, MITOCHONDRIAL RESPIRATORY CHAIN, DEFICIENCY OF *220111 : LEIGH SYNDROME, FRENCH-CANADIAN TYPE; LSFC *220120 : D-GLYCERICACIDEMIA #220150 : HYPOURICEMIA, RENAL 220200 : DANDY-WALKER SYNDROME; DWS *220210 : DANDY-WALKER-LIKE MALFORMATION WITH ATRIOVENTRICULAR SEPTAL DEFECT 220219 : DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY 220220 : DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY #220290 : DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 1; DFNB1 220300 : DEAFNESS, CONGENITAL, AND FAMILIAL MYOCLONIC EPILEPSY #220400 : JERVELL AND LANGE-NIELSEN SYNDROME; JLNS1 *220500 : DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, RECESSIVE FORM 220600 : DEAFNESS, CONGENITAL, AND SPLIT HANDS AND FEET #220700 : DEAFNESS, AUTOSOMAL RECESSIVE ^220800 : MOVED TO 220700 220900 : DEAFNESS, CONGENITAL, WITH TOTAL ALBINISM ^221000 : REMOVED FROM DATABASE 221200 : DEAFNESS, COCHLEAR, WITH MYOPIA AND INTELLECTUAL IMPAIRMENT *221300 : DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR 221320 : DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES *221350 : DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA 221400 : DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL AND PROGRESSIVE SENSORY NEUROPATHY 221500 : DEAFNESS, NEURAL, CONGENITAL MODERATE 221600 : DEAFNESS, NEURAL, EARLY ONSET *221650 : DEAFNESS, NEURAL, PROGRESSIVE CHILDHOOD TYPE 221700 : DEAFNESS, NEURAL, WITH ATYPICAL ATOPIC DERMATITIS 221740 : DEAFNESS-OLIGODONTIA SYNDROME *221745 : MITOCHONDRIAL DEAFNESS MODIFIER GENE 1; MDM1 221750 : DEAFNESS, SENSORINEURAL, WITH PITUITARY DWARFISM 221760 : DERMATOGLYPHICS--PALMAR TRIRADIUS d, ABSENCE OF #221770 : POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL 221780 : DERMATOGLYPHICS--HYPOTHENAR RADIAL ARCH 221790 : DERMATOLEUKODYSTROPHY *221800 : DERMOCHONDROCORNEAL DYSTROPHY 221810 : DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE 221820 : GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL *221900 : RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC 221950 : DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA 221995 : DIABETES INSIPIDUS, NEPHROGENIC, WITH MENTAL RETARDATION AND INTRACEREBRAL CALCIFICATION #222000 : DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL RECESSIVE *222100 : DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM #222300 : WOLFRAM SYNDROME 222350 : DIAMINOPENTANURIA 222400 : DIAPHRAGM, UNILATERAL AGENESIS OF 222448 : DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM, MYOPIA, AND SENSORINEURAL DEAFNESS 222470 : DIARRHEA, FATAL INFANTILE, WITH ABNORMAL HAIR 222500 : DIASTEMATOMYELIA #222600 : DIASTROPHIC DYSPLASIA *222690 : DIBASICAMINOACIDURIA I #222700 : LYSINURIC PROTEIN INTOLERANCE; LPI 222730 : DICARBOXYLICAMINOACIDURIA *222745 : 2,4-@DIENOYL-CoA REDUCTASE 1; DECR1 *222748 : DIHYDROPYRIMIDINASE; DPYS 222760 : DIGITORENOCEREBRAL SYNDROME #222765 : RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2; RCDP2 *222800 : DIPHOSPHOGLYCERATE MUTASE DEFICIENCY OF ERYTHROCYTE *222900 : DISACCHARIDE INTOLERANCE I *223000 : LACTASE DEFICIENCY, CONGENITAL #223100 : HYPOLACTASIA, ADULT TYPE 223200 : DISORGANIZATION, MOUSE, HOMOLOG OF 223300 : DISSEMINATED SCLEROSIS WITH NARCOLEPSY 223320 : DIVERTICULOSIS, SMALL-INTESTINAL 223330 : DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT 223340 : DK--PHOCOMELIA SYNDROME 223350 : DOHLE BODIES AND LEUKEMIA *223360 : DOPAMINE BETA-HYDROXYLASE, PLASMA; DBH *223370 : DUBOWITZ SYNDROME 223380 : DOPAMINE BETA-HYDROXYLASE, PLASMA, THERMOLABILITY OF 223400 : DUODENAL ATRESIA 223500 : DWARFISM, LOW-BIRTH-WEIGHT TYPE, WITH UNRESPONSIVENESS TO GROWTH HORMONE 223540 : DWARFISM, MENTAL RETARDATION, AND EYE ABNORMALITY 223550 : DWARFISM, PROPORTIONATE, WITH HIP DISLOCATION ^223600 : MOVED TO 127100 223610 : DWARFISM, SHORT-LIMB, WITH ABSENT FIBULAS AND VERY SHORT DIGITS *223800 : DYGGVE-MELCHIOR-CLAUSEN DISEASE #223900 : DYSAUTONOMIA, FAMILIAL; DYS 224000 : DYSAUTONOMIA-LIKE DISORDER *224050 : DYSEQUILIBRIUM SYNDROME; DES *224100 : ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II; CDAN2 *224120 : ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE I; CDAN1 224200 : DYSGENESIS MESODERMALIS CORNEAE ET SCLERAE 224230 : DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 224250 : DYSMYELINATION WITH JAUNDICE *224300 : DYSOSTEOSCLEROSIS 224400 : DYSSEGMENTAL DWARFISM #224410 : DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH *224500 : DYSTONIA MUSCULORUM DEFORMANS 2; DYT2 224550 : DYSTONIA WITH RINGBINDEN 224570 : DYSTONIA, FAMILIAL, WITH VISUAL FAILURE AND STRIATAL LUCENCIES 224600 : DYSTONIA, PERIODIC KINESIGENIC *224690 : EAR, PATELLA, SHORT STATURE SYNDROME 224700 : EBSTEIN ANOMALY *224750 : SCHOPF-SCHULZ-PASSARGE SYNDROME 224800 : ECTODERMAL DYSPLASIA AND NEUROSENSORY DEAFNESS #224900 : ECTODERMAL DYSPLASIA, ANHIDROTIC #225000 : CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1 225040 : ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESIS OF THE CORPUS CALLOSUM 225050 : ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARY DYSKINESIA #225060 : ECTODERMAL DYSPLASIA, MARGARITA ISLAND TYPE 225100 : ECTOPIA LENTIS *225200 : ECTOPIA LENTIS WITH ECTOPIA OF PUPIL ^225250 : MOVED TO 218700 *225280 : EEM SYNDROME 225290 : ECTRODACTYLY-POLYDACTYLY 225300 : ECTRODACTYLY 225310 : EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTIN ABNORMALITY 225320 : EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, TYPE UNSPECIFIED ^225350 : MOVED TO 130050 ^225360 : REMOVED FROM DATABASE #225400 : EHLERS-DANLOS SYNDROME, TYPE VI #225410 : EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE 225450 : ELLIPTOCYTOSIS, ATYPICAL #225500 : ELLIS-VAN CREVELD SYNDROME; EVC 225700 : ENCEPHALOMALACIA, MULTILOCULAR 225740 : ENCEPHALOPATHY, AXONAL, WITH NECROTIZING MYOPATHY, CARDIOMYOPATHY, AND CATARACTS *225750 : AICARDI-GOUTIERES SYNDROME 1; AGS1 225753 : ENCEPHALOPATHY, FATAL INFANTILE, WITH OLIVOPONTOCEREBELLAR HYPOPLASIA 225755 : ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION *225790 : ENCEPHALOCLASTIC PROLIFERATIVE VASCULOPATHY; EPV ^225795 : MOVED TO 166000 226000 : ENDOCARDIAL FIBROELASTOSIS; EFE 226100 : ENDOCARDIAL FIBROELASTOSIS AND COARCTATION OF ABDOMINAL AORTA 226110 : ENDOTHELIAL DYSTROPHY, CONGENITAL HEREDITARY, WITH NAIL HYPOPLASIA 226150 : ENTEROCOLITIS #226200 : ENTEROKINASE DEFICIENCY *226300 : ENTEROPATHY, PROTEIN-LOSING 226350 : EOSINOPHILIC FASCIITIS *226400 : EPIDERMODYSPLASIA VERRUCIFORMIS; EV 226440 : EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTAL RETARDATION *226450 : EPIDERMOLYSIS BULLOSA INVERSA DYSTROPHICA *226500 : EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA #226600 : EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1 #226650 : EPIDERMOLYSIS BULLOSA JUNCTIONALIS, DISENTIS TYPE #226670 : EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY #226700 : EPIDERMOLYSIS BULLOSA LETALIS #226730 : EPIDERMOLYSIS BULLOSA LETALIS WITH PYLORIC ATRESIA 226735 : EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA *226750 : EPILEPSY AND YELLOW TEETH 226800 : EPILEPSY, PHOTOGENIC, WITH SPASTIC DIPLEGIA AND MENTAL RETARDATION 226810 : EPILEPSY WITH BILATERAL OCCIPITAL CALCIFICATIONS 226850 : EPILEPSY-TELANGIECTASIA #226900 : EPIPHYSEAL DYSPLASIA, MULTIPLE, 4; EDM4 226950 : EPIPHYSEAL DYSPLASIA OF FEMORAL HEAD, MYOPIA, AND DEAFNESS *226960 : EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS #226980 : EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS 226985 : EPITHELIAL SQUAMOUS DYSPLASIA, KERATINIZING DESQUAMATIVE, OF URINARY TRACT 226990 : EPSTEIN-BARR VIRUS, SUSCEPTIBILITY TO CHRONIC INFECTION BY 227000 : ERYTHEMA OF ACRAL REGIONS 227010 : ERMINE PHENOTYPE 227050 : ERYTHROBLASTOPENIA, TRANSIENT *227090 : ERYTHRODERMA, LETHAL CONGENITAL 227100 : ERYTHRODERMA DESQUAMATIVA OF LEINER *227150 : ETHANOLAMINOSIS 227200 : EUNUCHOIDISM, FAMILIAL HYPOGONADOTROPHIC 227210 : EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY *227220 : EYE COLOR 3; EYCL3 *227240 : EYE COLOR 1; EYCL1 227250 : FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION 227255 : FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS *227260 : FACIAL ECTODERMAL DYSPLASIA 227270 : FACIOCARDIOMELIC DYSPLASIA, LETHAL 227280 : FACIOCARDIORENAL SYNDROME 227290 : FACIOOCULOACOUSTICORENAL SYNDROME ^227295 : MOVED TO 211910 #227300 : FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF; F5F8D 227310 : FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, WITH NORMAL PROTEIN C AND PROTEIN C INHIBITOR 227320 : FACIOTHORACOGENITAL SYNDROME *227330 : FACIODIGITOGENITAL SYNDROME, RECESSIVE *227400 : FACTOR V DEFICIENCY *227500 : FACTOR VII DEFICIENCY *227600 : FACTOR X DEFICIENCY *227645 : FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC *227646 : FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2 *227650 : FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA *227660 : FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB ^227700 : MOVED TO 134600 ^227800 : MOVED TO 134600 #227810 : FANCONI-BICKEL SYNDROME; FBS 227850 : FANCONI-LIKE SYNDROME *228000 : FARBER LIPOGRANULOMATOSIS 228020 : FASCIAL DYSTROPHY, CONGENITAL *228100 : FATTY METAMORPHOSIS OF VISCERA 228200 : FEMUR-FIBULA-ULNA SYNDROME *228250 : FEMUR, UNILATERAL BIFID, WITH MONODACTYLOUS ECTRODACTYLY #228300 : FERTILE EUNUCH SYNDROME 228355 : FETAL IODINE DEFICIENCY DISORDER; FIDD 228400 : FEVER, FAMILIAL LIFELONG PERSISTENT *228520 : FIBROCHONDROGENESIS 228550 : FIBROMATOSIS, CONGENITAL GENERALIZED; CGF 228560 : FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES *228600 : FIBROMATOSIS, JUVENILE HYALINE 228800 : FIBROSCLEROSIS, MULTIFOCAL *228900 : FIBULA APLASIA AND COMPLEX BRACHYDACTYLY 228930 : FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY 228940 : FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES *228960 : FLAUJEAC FACTOR DEFICIENCY 228980 : FLECK RETINA, FAMILIAL BENIGN 228990 : FLECK RETINA OF KANDORI *229000 : FLETCHER FACTOR DEFICIENCY 229045 : FOCAL EPITHELIAL HYPERPLASIA, ORAL *229050 : FOLIC ACID, TRANSPORT DEFECT INVOLVING 229070 : FOLLICLE-STIMULATING HORMONE, ISOLATED DEFICIENCY OF *229100 : FORMIMINOTRANSFERASE DEFICIENCY 229120 : FOUNTAIN SYNDROME 229150 : FRAGILE X, SUPPRESSOR OF *229200 : FRAGILITAS OCULI WITH JOINT HYPEREXTENSIBILITY 229230 : FRASER-LIKE SYNDROME 229250 : FREESIA FLOWERS, INABILITY TO SMELL #229300 : FRIEDREICH ATAXIA 1; FRDA 229310 : FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA *229400 : FRONTOFACIONASAL DYSOSTOSIS *229500 : FRUCTOSE AND GALACTOSE INTOLERANCE *229600 : FRUCTOSE INTOLERANCE, HEREDITARY 229650 : FRUCTOSE UTILIZATION *229700 : FRUCTOSE-1,6-BISPHOPHATASE 1; FBP1 *229800 : FRUCTOSURIA *229850 : FRYNS SYNDROME; FRNS 229900 : FUCHS ATROPHIA GYRATA CHORIOIDEAE ET RETINAE ^229950 : MOVED TO 136820 *230000 : FUCOSIDOSIS #230200 : GALACTOKINASE DEFICIENCY 230300 : GALACTORRHEA #230350 : GALACTOSE EPIMERASE DEFICIENCY #230400 : GALACTOSEMIA 230430 : GALACTOSYLTRANSFERASE DEFICIENCY #230450 : GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO *230500 : GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I #230600 : GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II, OR JUVENILE TYPE #230650 : GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III, OR ADULT TYPE *230700 : GANGLIOSIDOSIS, GM2, TYPE III, OR JUVENILE TYPE 230710 : GANGLIOSIDOSIS, GM2, JUVENILE, A(M)B VARIANT *230740 : GAPO SYNDROME 230750 : GASTROSCHISIS #230800 : GAUCHER DISEASE, TYPE I #230900 : GAUCHER DISEASE, TYPE II #231000 : GAUCHER DISEASE, TYPE III #231005 : GAUCHER-LIKE DISEASE *231050 : GELEOPHYSIC DYSPLASIA 231060 : GENITOPALATOCARDIAC SYNDROME *231070 : GERODERMA OSTEODYSPLASTICA; GO 231080 : GERMAN SYNDROME *231090 : HYDATIDIFORM MOLE 231095 : GHOSAL HEMATODIAPHYSEAL DYSPLASIA; GHDD #231100 : GIANT CELL HEPATITIS, NEONATAL *231200 : GIANT PLATELET SYNDROME #231300 : GLAUCOMA 3, PRIMARY INFANTILE, A; GLC3A ^231400 : REMOVED FROM DATABASE ^231500 : MOVED TO 231300 231520 : GLOOMY FACE SYNDROME 231530 : GLUCAGON DEFICIENCY, HYPOGLYCEMIA DUE TO #231550 : ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAA *231610 : GLUCURONIDASE, MOUSE, MODIFIER OF; GUSM 231630 : GLUTAMATE MONOSODIUM SENSITIVITY *231670 : GLUTARICACIDEMIA I *231675 : GLUTARICACIDURIA IIC *231680 : GLUTARICACIDURIA IIA 231690 : GLUTARYL-CoA OXIDASE DEFICIENCY #231900 : GLUTATHIONE SYNTHETASE DEFICIENCY OF ERYTHROCYTES, HEMOLYTIC ANEMIA DUE TO *231950 : GLUTATHIONURIA 231970 : GLUTEAL MUSCLES, ABSENCE OF *232000 : PROPIONYL-CoA CARBOXYLASE, ALPHA SUBUNIT; PCCA *232050 : PROPIONYL-CoA CARBOXYLASE, BETA SUBUNIT; PCCB *232200 : GLYCOGEN STORAGE DISEASE I ^232210 : MOVED TO 232200 #232220 : GLYCOGEN STORAGE DISEASE Ib #232240 : GLYCOGEN STORAGE DISEASE Ic #232300 : GLYCOGEN STORAGE DISEASE II ^232330 : MOVED TO 300257 *232400 : GLYCOGEN STORAGE DISEASE III *232500 : GLYCOGEN STORAGE DISEASE IV *232600 : GLYCOGEN STORAGE DISEASE V *232700 : GLYCOGEN STORAGE DISEASE VI *232800 : GLYCOGEN STORAGE DISEASE VII 232900 : GLYCOPROTEIN STORAGE DISEASE *233100 : RENAL GLUCOSURIA; GLYS1 233270 : GOMBO SYNDROME #233300 : PREMATURE OVARIAN FAILURE, AUTOSOMAL RECESSIVE *233400 : GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS 233420 : GONADAL DYSGENESIS, XY TYPE 233430 : GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES 233450 : GOODPASTURE SYNDROME 233500 : GORLIN-CHAUDHRY-MOSS SYNDROME 233600 : GRANULOCYTOPENIA WITH IMMUNOGLOBULIN ABNORMALITY 233650 : GRANULOMATOUS DISEASE DUE TO COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS 233670 : GRANULOMATOUS DISEASE WITH DEFECT IN NEUTROPHIL CHEMOTAXIS *233690 : GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL CYTOCHROME-b-NEGATIVE FORM *233700 : GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL CYTOCHROME-b-POSITIVE FORM I *233710 : GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL CYTOCHROME-b-POSITIVE FORM II 233800 : GROUPED PIGMENTATION OF THE MACULA 233805 : GROWTH FACTORS, COMBINED DEFECT OF 233810 : GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA #233910 : GTP CYCLOHYDROLASE I DEFICIENCY *234000 : HAGEMAN FACTOR DEFICIENCY 234030 : HAIR DEFECT WITH PHOTOSENSITIVITY AND MENTAL RETARDATION *234050 : HAIR-BRAIN SYNDROME 234100 : HALLERMANN-STREIFF SYNDROME; HSS #234200 : PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION; PKAN 234250 : HALL-RIGGS MENTAL RETARDATION SYNDROME 234280 : HALLUX VARUS AND PREAXIAL POLYSYNDACTYLY 234300 : HALO NEVI 234350 : HALOTHANE HEPATITIS *234500 : HARTNUP DISORDER 234580 : HEARING LOSS, SENSORINEURAL, WITH ENAMEL HYPOPLASIA AND NAIL DEFECTS 234700 : HEART BLOCK, CONGENITAL 234750 : HEART, MALFORMATION OF 234800 : HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES 234810 : HEMANGIOMATOSIS, FAMILIAL PULMONARY CAPILLARY 234820 : HEMANGIOPERICYTOMA, MALIGNANT 235000 : HEMIHYPERTROPHY *235200 : HEMOCHROMATOSIS; HFE *235255 : MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY 235360 : HEMOLYTIC ANEMIA, CONGENITAL, WITH EMPHYSEMA AND CUTIS LAXA 235370 : HEMOLYTIC ANEMIA WITH THERMAL SENSITIVITY OF RED CELLS #235400 : HEMOLYTIC-UREMIC SYNDROME; HUS 235500 : HEMOSIDEROSIS, PULMONARY, WITH DEFICIENCY OF GAMMA-A GLOBULIN *235510 : HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 235550 : HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNE DEFICIENCY 235555 : HEPATITIS, NEONATAL CHOLESTATIC, DUE TO DEFICIENCY OF DELTA(4)-3-OXOSTEROID 5-BETA-REDUCTASE 235600 : HERMAPHRODITISM, TRUE #235700 : HEXOKINASE DEFICIENCY HEMOLYTIC ANEMIA #235730 : HIRSCHSPRUNG DISEASE SYNDROME ^235735 : MOVED TO 277580 235740 : HIRSCHSPRUNG DISEASE WITH POLYDACTYLY, RENAL AGENESIS, AND DEAFNESS 235750 : HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIG TOES, AND VENTRICULAR SEPTAL DEFECT 235760 : HIRSCHSPRUNG DISEASE WITH HYPOPLASTIC NAILS AND DYSMORPHIC FACIAL FEATURES *235800 : HISTIDINEMIA *235830 : HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT *235900 : HISTIOCYTOSIS, FAMILIAL LIPOCHROME 236000 : HODGKIN LYMPHOMA *236100 : HOLOPROSENCEPHALY 1, ALOBAR; HPE1 236110 : HOLZGREVE SYNDROME 236130 : HOMOCARNOSINOSIS *236200 : HOMOCYSTINURIA #236250 : HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY #236270 : HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA DUE TO DEFECT IN COBALAMIN METABOLISM, cbl E COMPLEMENTATION TYPE 236300 : HOOFT DISEASE *236400 : HUMERORADIAL SYNOSTOSIS 236410 : HUMERORADIAL/MULTIPLE SYNOSTOSIS SYNDROME 236450 : HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME 236490 : HYALINOSIS, SYSTEMIC INFANTILE 236500 : HYDRANENCEPHALY WITH RENAL APLASIA-DYSPLASIA 236600 : HYDROCEPHALUS 236635 : HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS 236640 : HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS 236660 : HYDROCEPHALUS, TALL STATURE, JOINT LAXITY, AND KYPHOSCOLIOSIS *236670 : WALKER-WARBURG SYNDROME *236680 : HYDROLETHALUS SYNDROME 236690 : HYDROCEPHALUS, NORMAL-PRESSURE #236700 : MCKUSICK-KAUFMAN SYNDROME; MKKS *236730 : UROFACIAL SYNDROME; UFS 236750 : HYDROPS FETALIS, IDIOPATHIC *236792 : L-2-@HYDROXYGLUTARICACIDEMIA *236795 : 3-@HYDROXYISOBUTYRICACIDURIA *236800 : HYDROXYKYNURENINURIA *236900 : HYDROXYLYSINURIA 237000 : HYDROXYPROLINEMIA 237100 : HYMEN, IMPERFORATE *237300 : HYPERAMMONEMIA DUE TO CARBAMOYLPHOSPHATE SYNTHETASE I DEFICIENCY *237310 : HYPERAMMONEMIA DUE TO N-ACETYLGLUTAMATE SYNTHETASE DEFICIENCY 237400 : HYPER-BETA-ALANINEMIA *237450 : HYPERBILIRUBINEMIA, ROTOR TYPE #237500 : DUBIN-JOHNSON SYNDROME; DJS 237550 : HYPERBILIRUBINEMIA, CONJUGATED, TYPE III *237800 : HYPERBILIRUBINEMIA, SHUNT #237900 : HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATAL 238200 : HYPERCYSTINURIA, ISOLATED *238300 : GLYCINE DECARBOXYLASE; GLDC *238310 : AMINOMETHYLTRANSFERASE; AMT *238320 : HYPERGONADOTROPIC HYPOGONADISM; HHG *238330 : GLYCINE CLEAVAGE SYSTEM H PROTEIN; GCSH *238331 : GLYCINE CLEAVAGE SYSTEM L PROTEIN; GCSL 238340 : HYPERLEUCINE-ISOLEUCINEMIA 238350 : HYPERLEXIA 238400 : HYPERLIPIDEMIA, TYPE V 238500 : HYPERLIPIDEMIA, TYPE VI *238600 : HYPERLIPOPROTEINEMIA, TYPE I #238700 : HYPERLYSINEMIA 238710 : HYPERLYSINEMIA DUE TO DEFECT IN LYSINE TRANSPORT INTO MITOCHONDRIA 238750 : HYPERLYSINURIA WITH HYPERAMMONEMIA 238800 : HYPERMETABOLISM DUE TO DEFECT IN MITOCHONDRIA 238950 : HYPEROPIA, HIGH #238970 : HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME *239000 : HYPEROSTOSIS CORTICALIS DEFORMANS JUVENILIS *239100 : HYPEROSTOSIS CORTICALIS GENERALISATA 239199 : HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA #239200 : HYPERPARATHYROIDISM, NEONATAL SEVERE PRIMARY; NSHPT *239300 : HYPERPHOSPHATASIA WITH MENTAL RETARDATION 239350 : HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES 239400 : HYPERPIPECOLATEMIA *239500 : HYPERPROLINEMIA, TYPE I #239510 : HYPERPROLINEMIA, TYPE II 239710 : ACROFRONTOFACIONASAL DYSOSTOSIS, SEVERE 239711 : HYPERTELORISM AND TETRALOGY OF FALLOT *239800 : HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME 239840 : HYPERTRICHOSIS, CONGENITAL ANTERIOR CERVICAL, WITH PERIPHERAL SENSORY AND MOTOR NEUROPATHY 239850 : HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA 239900 : HYPERTROPHIC NEUROPATHY AND CATARACT 240000 : HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 240100 : HYPERURICEMIA, LIPODYSTROPHY, AND NEUROLOGIC DEFECT 240150 : HYPERVITAMINOSIS A, SUSCEPTIBILITY TO *240200 : HYPOADRENOCORTICISM, FAMILIAL *240300 : AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I 240400 : HYPOASCORBEMIA *240500 : COMMON VARIABLE IMMUNODEFICIENCY #240600 : GLYCOGEN STORAGE DISEASE 0 240800 : HYPOGLYCEMIA, LEUCINE-INDUCED 240900 : HYPOGLYCEMIA, NEONATAL, SIMULATING FOETOPATHIA DIABETICA 240950 : HYPOGONADISM-CATARACT SYNDROME 241000 : HYPOGONADISM WITH LOW-GRADE MENTAL DEFICIENCY AND MICROCEPHALY *241080 : HYPOGONADISM, DIABETES MELLITUS, ALOPECIA, MENTAL RETARDATION, AND ELECTROCARDIOGRAPHIC ABNORMALITIES 241090 : HYPOGONADISM, PRIMARY, AND PARTIAL ALOPECIA 241100 : HYPOGONADISM, MALE 241120 : HYPOHIDROSIS WITH ABNORMAL PALMAR DERMAL RIDGES *241150 : HYPOKALEMIA, FAMILIAL #241200 : HYPOKALEMIC ALKALOSIS WITH HYPERCALCIURIA *241310 : HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS *241400 : HYPOPARATHYROIDISM *241410 : HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRD #241500 : HYPOPHOSPHATASIA, INFANTILE #241510 : HYPOPHOSPHATASIA, CHILDHOOD 241519 : HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS 241520 : HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE *241530 : HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY; HHRH 241540 : HYPOPITUITARISM, CONGENITAL, WITH CENTRAL DIABETES INSIPIDUS 241550 : HYPOPLASTIC LEFT HEART SYNDROME 241600 : HYPOPROTEINEMIA, HYPERCATABOLIC 241750 : HYPOSPADIAS 241760 : HYPOSPADIAS-MENTAL RETARDATION SYNDROME 241800 : HYPOTHALAMIC HAMARTOMAS #241850 : HYPOTHYROIDISM, ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE ^241900 : MOVED TO 203655 242050 : HYPOURICEMIA, HYPERCALCINURIA, AND DECREASED BONE DENSITY #242100 : ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1; NCIE1 242150 : ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS ^242170 : MOVED TO 601675 #242300 : ICHTHYOSIS, LAMELLAR, 1; LI1 242400 : ICHTHYOSIS CONGENITA WITH BILIARY ATRESIA *242500 : ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE 242510 : ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION 242520 : ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION 242530 : ICHTHYOSIS, MENTAL RETARDATION, DWARFISM, AND RENAL IMPAIRMENT 242550 : ICHTHYOSIS, SPLIT HAIRS, AND AMINOACIDURIA *242600 : IMINOGLYCINURIA #242650 : PRIMARY CILIARY DYSKINESIA; PCD *242670 : IMMOTILE CILIA SYNDROME DUE TO DEFECTIVE RADIAL SPOKES 242680 : IMMOTILE CILIA SYNDROME DUE TO EXCESSIVELY LONG CILIA *242700 : IMMUNE DEFECT DUE TO ABSENCE OF THYMUS ^242800 : REMOVED FROM DATABASE *242840 : IMMUNODEFICIENCY WITH CLEFT LIP/PALATE, CATARACT, HYPOPIGMENTATION, AND ABSENT CORPUS CALLOSUM 242850 : IMMUNE DEFICIENCY DISEASE #242860 : IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 242870 : IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTS AND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES 242880 : IMMUNOERYTHROMYELOID HYPOPLASIA 242890 : IMMUNOGLOBULIN D LEVEL IN PLASMA, LOW #242900 : IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE *243000 : INDIFFERENCE TO PAIN 243050 : INDOLYLACROYL GLYCINURIA WITH MENTAL RETARDATION 243060 : INFERTILITY ASSOCIATED WITH MULTI-TAILED SPERMATOZOA AND EXCESSIVE DNA 243080 : INOSINE PHOSPHORYLASE DEFICIENCY, IMMUNE DEFECT DUE TO 243095 : INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO 243100 : INTERNAL CAROTID ARTERIES, HYPOPLASIA OF 243110 : INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO *243150 : INTESTINAL ATRESIA, MULTIPLE *243180 : INTESTINAL PSEUDOOBSTRUCTION DUE TO NEURONAL DISEASE 243185 : INTESTINAL PSEUDOOBSTRUCTION WITH PATENT DUCTUS ARTERIOSUS AND NATAL TEETH 243200 : INTRACRANIAL HYPERTENSION, IDIOPATHIC #243300 : CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC; BRIC *243305 : INVERSIN 243310 : IRIS COLOBOMA WITH PTOSIS, HYPERTELORISM, AND MENTAL RETARDATION 243320 : INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF 243340 : ISCHIADIC HYPOPLASIA WITH RENAL DYSFUNCTION, IMMUNODEFICIENCY, AND POLYDACTYLY *243400 : ISONIAZID INACTIVATION 243440 : ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME 243450 : ISOVALERIC ACID, INABILITY TO SMELL #243500 : ISOVALERICACIDEMIA; IVA *243600 : JEJUNAL ATRESIA 243605 : JEJUNAL ATRESIA WITH MICROCEPHALY AND OCULAR ANOMALIES 243700 : JOB SYNDROME *243800 : JOHANSON-BLIZZARD SYNDROME; JBS 243910 : JOUBERT SYNDROME WITH BILATERAL CHORIORETINAL COLOBOMA 244100 : JUMPING FRENCHMAN OF MAINE *244200 : KALLMANN SYNDROME 3; KAL3 244300 : KAPUR-TORIELLO SYNDROME #244400 : KARTAGENER SYNDROME *244450 : KAUFMAN OCULOCEREBROFACIAL SYNDROME *244460 : KENNY-CAFFEY SYNDROME, TYPE 1; KCS ^244500 : MOVED TO 148300 244510 : KERATOCONUS AND CONGENITAL HIP DYSPLASIA 244600 : KERATOCONUS POSTICUS CIRCUMSCRIPTUS; KPC 244850 : KERATODERMA, PALMOPLANTAR, NORRBOTTEN RECESSIVE TYPE #245000 : PAPILLON-LEFEVRE SYNDROME; PALS #245010 : HAIM-MUNK SYNDROME; HMS *245050 : 3-@OXOACID CoA TRANSFERASE; OXCT *245100 : KETOACIDURIA WITH MENTAL DEFICIENCY AND OTHER FEATURES 245130 : KETOADIPICACIDURIA #245150 : KEUTEL SYNDROME 245160 : KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS 245180 : KIFAFA SEIZURE DISORDER 245190 : KNIEST-LIKE DYSPLASIA, LETHAL #245200 : KRABBE DISEASE 245210 : KOUSSEFF SYNDROME 245300 : KURU 245340 : LACTATE TRANSPORTER DEFECT, MYOPATHY DUE TO 245348 : LACTIC ACIDEMIA DUE TO DEFECT OF E2 LIPOYL TRANSACETYLASE OF THE PYRUVATE DEHYDROGENASE COMPLEX *245349 : PYRUVATE DEHYDROGENASE COMPLEX, COMPONENT X *245400 : LACTIC ACIDOSIS, CONGENITAL INFANTILE 245450 : LACTIC ACIDURIA DUE TO D-LACTIC ACID #245480 : SPECIFIC GRANULE DEFICIENCY; SGD ^245500 : REMOVED FROM DATABASE 245550 : LAMBERT SYNDROME 245552 : LAMBOTTE SYNDROME 245570 : LANDAU-KLEFFNER SYNDROME; LKS 245590 : LARON SYNDROME, TYPE II *245600 : LARSEN SYNDROME, RECESSIVE 245650 : LARSEN-LIKE SYNDROME, LETHAL TYPE *245660 : LARYNGOONYCHOCUTANEOUS SYNDROME; LOCS *245800 : LAURENCE-MOON SYNDROME #245900 : LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY *246000 : LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT #246200 : LEPRECHAUNISM *246300 : LEPROSY, SUSCEPTIBILITY TO *246400 : LETTERER-SIWE DISEASE *246450 : 3-@HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY 246470 : LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER ^246490 : MOVED TO 266265 246500 : LEUKOMELANODERMA, INFANTILISM, MENTAL RETARDATION, HYPODONTIA, HYPOTRICHOSIS *246530 : LEUKOTRIENE C4 SYNTHASE; LTC4S 246550 : LICHTENSTEIN SYNDROME 246555 : LIMB DEFECTS, DISTAL TRANSVERSE, WITH MENTAL RETARDATION AND SPASTICITY 246560 : LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA 246570 : LIMB DEFICIENCY-HEART MALFORMATION SYNDROME *246600 : LIPASE, CONGENITAL ABSENCE OF PANCREATIC 246650 : LIPASE DEFICIENCY, COMBINED *246700 : LIPID TRANSPORT DEFECT OF INTESTINE *246800 : LIPIDOSIS, JUVENILE DYSTONIC *246900 : LIPOAMIDE DEHYDROGENASE DEFICIENCY, LACTIC ACIDOSIS DUE TO #247100 : LIPOID PROTEINOSIS OF URBACH AND WIETHE 247150 : LIP PRINTS #247200 : MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS ^247400 : MOVED TO 210710 247410 : LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME 247420 : LUTHERAN NULL 247430 : LYMPHOBLASTIC TRANSFORMATION, INHIBITION OF 247440 : LYMPHEDEMA, CONGENITAL RECESSIVE 247450 : LYMPHOBLASTIC TRANSFORMATION, INTRINSIC DEFECT IN 247610 : LYMPHOID INTERSTITIAL PNEUMONIA; LIP 247630 : LYMPHOID SYSTEM DETERIORATION, PROGRESSIVE 247640 : LYMPHOBLASTIC LEUKEMIA, ACUTE, WITH LYMPHOMATOUS FEATURES; LALL 247650 : LYMPHOKINE DEFICIENCY *247800 : LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNE HEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS ^247900 : MOVED TO 238700 247950 : LYSINE MALABSORPTION SYNDROME *247980 : LIPASE B, LYSOSOMAL ACID; LIPB 247990 : MACDERMOT-WINTER SYNDROME 248000 : MACROCEPHALY 248010 : MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE 248100 : MACROSOMIA ADIPOSA CONGENITA 248110 : MACROSOMIA WITH MICROPHTHALMIA, LETHAL 248190 : MACULAR COLOBOMA, BILATERAL, WITH HYPERCALCIURIA #248200 : STARGARDT DISEASE 1; STGD1 #248250 : HYPOMAGNESEMIA, PRIMARY 248260 : MAGNESIUM, ELEVATED RED CELL #248300 : MAL DE MELEDA *248310 : MALARIA, INTENSITY OF INFECTION IN 248340 : MALPUECH FACIAL CLEFTING SYNDROME 248350 : MALOCCLUSION AND SHORT STATURE #248360 : MALONYL-CoA DECARBOXYLASE DEFICIENCY *248370 : MANDIBULOACRAL DYSPLASIA; MAD 248390 : MANDIBULOFACIAL DYSOSTOSIS, TREACHER COLLINS TYPE, AUTOSOMAL RECESSIVE 248400 : MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL DEFICIENCY 248450 : MANITOBA OCULOTRICHOANAL SYNDROME; MOTA *248500 : MANNOSIDOSIS, ALPHA B, LYSOSOMAL *248510 : MANNOSIDOSIS, BETA A, LYSOSOMAL *248600 : MAPLE SYRUP URINE DISEASE, TYPE IA *248610 : MAPLE SYRUP URINE DISEASE, TYPE II *248611 : MAPLE SYRUP URINE DISEASE, TYPE IB *248700 : MARDEN-WALKER SYNDROME ^248750 : MOVED TO 154700 248760 : MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS 248770 : MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL *248800 : MARINESCO-SJOGREN SYNDROME; MSS 248810 : MARINESCO-SJOGREN-LIKE SYNDROME; MSLS *248900 : MAST SYNDROME 248910 : MASTOCYTOSIS, CUTANEOUS, WITH SHORT STATURE, CONDUCTIVE HEARING LOSS AND MICROTIA 248950 : MCDONOUGH SYNDROME *249000 : MECKEL SYNDROME, TYPE 1; MKS1 *249100 : FAMILIAL MEDITERRANEAN FEVER; FMF *249210 : MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 249230 : MEGAEPIPHYSEAL DWARFISM 249240 : MEGALENCEPHALY WITH DYSMYELINATION #249270 : THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA 249300 : MEGALOCORNEA *249310 : MEGALOCORNEA-MENTAL RETARDATION SYNDROME 249400 : MELANOSIS, NEUROCUTANEOUS 249420 : MELNICK-NEEDLES SYNDROME 249500 : MENTAL RETARDATION, RECESSIVE 249599 : MENTAL RETARDATION SYNDROME, BELGIAN TYPE 249600 : MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE *249620 : MENTAL RETARDATION, CONGENITAL HEART DISEASE, BLEPHAROPHIMOSIS, BLEPHAROPTOSIS, AND HYPOPLASTIC TEETH 249630 : MENTAL RETARDATION, BUENOS AIRES TYPE *249650 : MERCAPTOLACTATE-CYSTEINE DISULFIDURIA; MCDU 249660 : MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES 249670 : MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION #249700 : LANGER MESOMELIC DYSPLASIA 249710 : MESOMELIC LIMB SHORTENING AND BOWING 249800 : METACHROMATIC LEUKODYSTROPHY AND AMAUROTIC IDIOCY, COMBINED FEATURES OF #249900 : METACHROMATIC LEUKODYSTROPHY DUE TO DEFICIENCY OF CEREBROSIDE SULFATASE ACTIVATOR *250100 : METACHROMATIC LEUKODYSTROPHY 250215 : METAPHYSEAL ACROSCYPHODYSPLASIA 250220 : METAPHYSEAL CHONDRODYSPLASIA, CONGENITAL LETHAL 250230 : METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE #250250 : CARTILAGE-HAIR HYPOPLASIA; CHH 250300 : METAPHYSEAL CHONDRODYSPLASIA, PENA TYPE 250400 : METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE 250410 : METAPHYSEAL CHONDRODYSPLASIA WITH RETINITIS PIGMENTOSA 250420 : METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS 250450 : METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY #250460 : METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS 250500 : METAPHYSEAL MODELING ABNORMALITY, SKIN LESIONS, AND SPASTIC PARAPLEGIA *250600 : METATROPIC DWARFISM *250620 : METHACRYLICACIDURIA 250650 : METHANE PRODUCTION 250700 : METHEMOGLOBIN REDUCTASE DEFICIENCY *250790 : METHEMOGLOBINEMIA DUE TO DEFICIENCY OF CYTOCHROME b5 *250800 : METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE *250850 : METHIONINE ADENOSYLTRANSFERASE DEFICIENCY *250900 : METHIONINE MALABSORPTION SYNDROME #250940 : METHYLCOBALAMIN DEFICIENCY, cbl G TYPE *250950 : 3-@METHYLGLUTACONICACIDURIA 250951 : 3-@METHYLGLUTACONICACIDURIA, TYPE IV *251000 : METHYLMALONICACIDURIA DUE TO METHYLMALONIC CoA MUTASE DEFICIENCY *251100 : METHYLMALONICACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN--cbl A *251110 : METHYLMALONICACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN--cbl B 251120 : METHYLMALONICACIDURIA III *251170 : MEVALONATE KINASE; MVK 251190 : MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE *251200 : MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1; MCPH1 251220 : MICROCEPHALY-CARDIOMYOPATHY *251230 : MICROCEPHALY-MICROMELIA SYNDROME 251240 : MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA 251250 : MICROCEPHALY WITH CERVICAL SPINE FUSION ANOMALIES 251255 : MICROCEPHALY WITH DIGITAL ANOMALIES #251260 : NIJMEGEN BREAKAGE SYNDROME *251270 : MICROCEPHALY WITH CHORIORETINOPATHY 251280 : MICROCEPHALY WITH SPASTIC QUADRIPLEGIA 251290 : PSEUDO-TORCH SYNDROME *251300 : MICROCEPHALY, HIATUS HERNIA, AND NEPHROTIC SYNDROME 251400 : MICROCOLON *251450 : MICROMELIC DWARFISM WITH VERTEBRAL AND METAPHYSEAL ABNORMALITIES AND ADVANCED CARPOTARSAL OSSIFICATION 251455 : MICROMELIC DYSPLASIA, CONGENITAL, WITH DISLOCATION OF RADIUS *251500 : MICROPHTHALMIA AND MENTAL DEFICIENCY 251505 : MICROPHTHALMIA WITH COLOBOMATOUS CYST *251600 : MICROPHTHALMOS, AUTOSOMAL RECESSIVE 251700 : MICROPHTHALMOS WITH HYPERMETROPIA, RETINAL DEGENERATION, MACROPHAKIA AND DENTAL ANOMALIES 251750 : MICROSPHEROPHAKIA *251800 : MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS *251850 : MICROVILLUS INCLUSION DISEASE #251880 : MITOCHONDRIAL DNA DEPLETION SYNDROME ^251890 : MOVED TO 143450 251900 : MITOCHONDRIAL MYOPATHY 251945 : MITOCHONDRIAL MYOPATHY WITH A DEFECT IN MITOCHONDRIAL-PROTEIN TRANSPORT 251950 : MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS #252010 : COMPLEX I, MITOCHONDRIAL RESPIRATORY CHAIN, DEFICIENCY OF 252011 : COMPLEX II, MITOCHONDRIAL RESPIRATORY CHAIN, DEFICIENCY OF 252030 : MITRAL VALVE PROLAPSE AND OPHTHALMOPLEGIA *252100 : MOHR SYNDROME #252150 : MOLYBDENUM COFACTOR DEFICIENCY ^252160 : MOVED TO 252150 252200 : MONILETHRIX 252250 : MONOCYTE CHEMOTACTIC DISORDER 252270 : MONOSOMY 7 OF BONE MARROW 252300 : MORQUIO SYNDROME, NONKERATOSULFATE-EXCRETING TYPE 252320 : MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA *252350 : MOYAMOYA DISEASE *252500 : MUCOLIPIDOSIS II *252600 : MUCOLIPIDOSIS III *252605 : MUCOLIPIDOSIS III, VARIANT FORM #252650 : MUCOLIPIDOSIS IV #252700 : MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES *252800 : MUCOPOLYSACCHARIDOSIS TYPE I #252900 : MUCOPOLYSACCHARIDOSIS TYPE IIIA *252920 : MUCOPOLYSACCHARIDOSIS TYPE IIIB *252930 : MUCOPOLYSACCHARIDOSIS TYPE IIIC *252940 : MUCOPOLYSACCHARIDOSIS TYPE IIID *253000 : MUCOPOLYSACCHARIDOSIS TYPE IVA #253010 : MUCOPOLYSACCHARIDOSIS TYPE IVB *253200 : MUCOPOLYSACCHARIDOSIS TYPE VI *253220 : MUCOPOLYSACCHARIDOSIS TYPE VII #253230 : MUCOPOLYSACCHARIDOSIS TYPE VIII *253240 : MUCUS INSPISSATION OF RESPIRATORY TRACT #253250 : MULIBREY NANISM *253260 : BIOTINIDASE; BTD *253270 : MULTIPLE CARBOXYLASE DEFICIENCY, BIOTIN-RESPONSIVE; MCD #253280 : MUSCLE-EYE-BRAIN DISEASE; MEB *253290 : MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE #253300 : SPINAL MUSCULAR ATROPHY I; SMA1 *253310 : LETHAL CONGENITAL CONTRACTURE SYNDROME 253320 : MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPIC HYPOGONADISM #253400 : SPINAL MUSCULAR ATROPHY III; SMA3 ^253500 : REMOVED FROM DATABASE #253550 : SPINAL MUSCULAR ATROPHY II; SMA2 253590 : MUSCULAR DYSTROPHY, ADULT-ONSET, WITH LEUKOENCEPHALOPATHY #253600 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A #253601 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B *253700 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C *253800 : FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY; FCMD 253850 : MUSCULAR DYSTROPHY, CONGENITAL, EICHSFELD TYPE *253900 : MUSCULAR DYSTROPHY, CONGENITAL, PRODUCING ARTHROGRYPOSIS 254000 : MUSCULAR DYSTROPHY, CONGENITAL, WITH INFANTILE CATARACT AND HYPOGONADISM #254090 : MUSCULAR DYSTROPHY, SCLEROATONIC 254100 : MUSCULAR DYSTROPHY, CONGENITAL, WITH RAPID PROGRESSION #254110 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H; LGMD2H 254120 : MUSCULAR HYPERTONIA, LETHAL #254130 : MIYOSHI MYOPATHY; MM *254150 : MUSK, INABILITY TO SMELL 254190 : MYASTHENIA, CONGENITAL, REFRACTORY TO ACETYLCHOLINESTERASE INHIBITORS 254195 : MYASTHENIA, CONGENITAL, PREDOMINANTLY FACIAL AND MASTICATORY 254200 : MYASTHENIA GRAVIS; MG #254210 : MYASTHENIA GRAVIS, FAMILIAL INFANTILE; FIMG 254300 : MYASTHENIC MYOPATHY 254400 : MYCOSIS FUNGOIDES 254450 : MYELOFIBROSIS, FAMILIAL #254500 : MYELOMA, MULTIPLE #254600 : MYELOPEROXIDASE DEFICIENCY 254700 : MYELOPROLIFERATIVE DISEASE, AUTOSOMAL RECESSIVE *254770 : MYOCLONIC EPILEPSY, JUVENILE, 1; EJM1 *254780 : EPILEPSY, PROGRESSIVE MYOCLONIC 2; EPM2A #254800 : MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG *254900 : MYOCLONUS-NEPHROPATHY SYNDROME 254940 : MYOPATHY, CONGENITAL NONPROGRESSIVE, WITH MOEBIUS SEQUENCE AND ROBIN SEQUENCE 254950 : MYOPATHY, GRANULOVACUOLAR LOBULAR, WITH ELECTRICAL MYOTONIA 254960 : MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT 255100 : MYOPATHY WITH ABNORMAL LIPID METABOLISM #255110 : MYOPATHY WITH DEFICIENCY OF CARNITINE PALMITOYLTRANSFERASE II #255120 : HYPOGLYCEMIA, HYPOKETOTIC, WITH DEFICIENCY OF CARNITINE PALMITOYLTRANSFERASE I *255125 : MYOPATHY WITH DEFICIENCY OF SUCCINATE DEHYDROGENASE AND ACONITASE 255140 : MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA 255160 : MYOPATHY WITH LYSIS OF TYPE I MYOFIBRILS ^255170 : MOVED TO 603280 255200 : MYOPATHY, CENTRONUCLEAR *255300 : MYOPATHY, CONGENITAL 255310 : MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION *255320 : MYOPATHY, CONGENITAL MULTICORE, WITH EXTERNAL OPHTHALMOPLEGIA 255500 : MYOPIA, INFANTILE SEVERE 255600 : MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL #255700 : MYOTONIA, GENERALIZED 255710 : MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION #255800 : SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1 255900 : MYXEDEMA #255960 : MYXOMA, INTRACARDIAC 255980 : NASODIGITOACOUSTIC SYNDROME 255990 : NATHALIE SYNDROME 255995 : NATIVE AMERICAN MYOPATHY #256000 : LEIGH SYNDROME; LS 256020 : NAIL-PATELLA-LIKE RENAL DISEASE #256030 : NEMALINE MYOPATHY 2, AUTOSOMAL RECESSIVE; NEM2 256040 : NAKAJO SYNDROME #256050 : NEONATAL OSSEOUS DYSPLASIA I *256100 : NEPHRONOPHTHISIS 1; NPHP1 256120 : NEPHROPATHY, DEAFNESS, AND HYPERPARATHYROIDISM 256150 : NEPHROSIALIDOSIS 256200 : NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS #256300 : NEPHROSIS 1, CONGENITAL, FINNISH TYPE; NPHS1 ^256340 : MOVED TO 146255 256350 : NEPHROTIC SYNDROME WITH FOCAL GLOMERULAR SCLEROSIS #256370 : NEPHROTIC SYNDROME, EARLY-ONSET, WITH DIFFUSE MESANGIAL SCLEROSIS #256450 : NESIDIOBLASTOSIS OF PANCREAS #256500 : NETHERTON SYNDROME; NETH *256520 : NEU-LAXOVA SYNDROME; NLS *256540 : NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY *256550 : NEURAMINIDASE DEFICIENCY *256600 : NEUROAXONAL DYSTROPHY, INFANTILE 256690 : NEUROFACIODIGITORENAL SYNDROME *256700 : NEUROBLASTOMA *256710 : NEUROECTODERMAL MELANOLYSOSOMAL DISEASE 256720 : NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY #256730 : CEROID LIPOFUSCINOSIS, NEURONAL 1, INFANTILE; CLN1 *256731 : CEROID LIPOFUSCINOSIS, NEURONAL 5; CLN5 #256800 : INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA *256810 : NEUROPATHY, CONGENITAL SENSORY, WITH NEUROTROPHIC KERATITIS 256840 : NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA #256850 : GIANT AXONAL NEUROPATHY 1; GAN1 256851 : NEUROPATHY, GIANT AXONAL, TUNISIAN FORM *256855 : NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH EXCESSIVE MYELIN FOLDING COMPLEX, AUTOSOMAL RECESSIVE 256860 : NEUROPATHY, HEREDITARY SENSORY, ATYPICAL 256870 : NEUROPATHY, PAINFUL 257000 : NEUROVISCERAL STORAGE DISEASE WITH CURVILINEAR BODIES 257050 : NEUROVISCERAL STORAGE DISEASE WITH VERTICAL SUPRANUCLEAR OPHTHALMOPLEGIA 257100 : NEUTROPENIA, LETHAL CONGENITAL, WITH EOSINOPHILIA *257150 : NEUTROPHIL ACTIN DYSFUNCTION; NAD *257200 : NIEMANN-PICK DISEASE *257220 : NIEMANN-PICK DISEASE, TYPE C #257250 : NIEMANN-PICK DISEASE WITHOUT SPHINGOMYELINASE DEFICIENCY *257270 : NIGHT BLINDNESS WITH HIGH-GRADE MYOPIA 257300 : NONDISJUNCTION #257320 : LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE 257350 : NUCHAL BLEB, FAMILIAL 257400 : NYSTAGMUS, CONGENITAL MOTOR, AUTOSOMAL RECESSIVE 257500 : OBESITY-HYPOVENTILATION SYNDROME *257550 : OCULAR MOTOR APRAXIA *257600 : OCULAR MYOPATHY WITH CURARE SENSITIVITY 257790 : OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS *257800 : OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION *257850 : OCULODENTOOSSEOUS DYSPLASIA, RECESSIVE 257910 : OCULOPALATOCEREBRAL DWARFISM 257920 : OCULOPALATOSKELETAL SYNDROME #257950 : MUSCULAR DYSTROPHY, OCULOPHARYNGEAL, AUTOSOMAL RECESSIVE 257960 : OCULOTRICHODYSPLASIA; OTD *257970 : OCULORENOCEREBELLAR SYNDROME 257980 : ODONTOONYCHODERMAL DYSPLASIA 258040 : OEIS COMPLEX #258100 : OGUCHI DISEASE ^258120 : MOVED TO 271245 *258150 : OLIGOSYNAPTIC INFERTILITY 258200 : OLIVER SYNDROME *258300 : OLIVOPONTOCEREBELLAR ATROPHY II 258315 : OMODYSPLASIA, GENERALIZED FORM 258320 : OMPHALOCELE-CLEFT PALATE SYNDROME, LETHAL *258360 : ONYCHOTRICHODYSPLASIA AND NEUTROPENIA *258400 : OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS 258450 : OPHTHALMOPLEGIA, PROGRESSIVE EXTERNAL 258470 : OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA *258480 : OPSISMODYSPLASIA 258500 : OPTIC ATROPHY, CONGENITAL OR EARLY INFANTILE #258501 : 3-@METHYLGLUTACONICACIDURIA, TYPE III 258650 : OPTIC ATROPHY, NERVE DEAFNESS, AND DISTAL NEUROGENIC AMYOTROPHY 258660 : OPTIC NEUROPATHY, ANTERIOR ISCHEMIC *258700 : OPTICOCOCHLEODENTATE DEGENERATION 258800 : ORAL SENSIBILITY, DISTURBANCE OF 258840 : ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS *258850 : ORAL-FACIAL-DIGITAL SYNDROME, TYPE III 258860 : ORAL-FACIAL-DIGITAL SYNDROME, TYPE IV 258865 : ORAL-FACIAL-DIGITAL SYNDROME WITH RETINAL ABNORMALITIES *258870 : ORNITHINE AMINOTRANSFERASE DEFICIENCY *258900 : OROTICACIDURIA I 258920 : OROTICACIDURIA II 259050 : OSSIFIED EAR CARTILAGES WITH MENTAL DEFICIENCY, MUSCLE WASTING, AND BONY CHANGES 259100 : OSTEOARTHROPATHY, FAMILIAL IDIOPATHIC, OF CHILDHOOD 259200 : OSTEOCHONDROSIS DEFORMANS TIBIAE, FAMILIAL INFANTILE TYPE *259250 : OSTEODYSPLASIA, FAMILIAL, ANDERSON TYPE 259270 : OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI ^259400 : MOVED TO 166210 259410 : OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS #259420 : OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE 259440 : OSTEOGENESIS IMPERFECTA, SILLENCE TYPE II/III, WITHOUT ABNORMALITY OF TYPE I COLLAGEN *259450 : BRUCK SYNDROME #259500 : OSTEOGENIC SARCOMA 259550 : OSTEOID OSTEOMA 259600 : OSTEOLYSIS, HEREDITARY MULTICENTRIC 259610 : OSTEOLYSIS SYNDROME, RECESSIVE 259650 : OSTEOMA OF MIDDLE EAR 259660 : OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION 259680 : OSTEOMYELITIS, CHRONIC MULTIFOCAL; OCM 259690 : OSTEOPENIA AND SPARSE HAIR #259700 : OSTEOPETROSIS, AUTOSOMAL RECESSIVE 259710 : OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM 259720 : OSTEOPETROSIS, LETHAL *259730 : OSTEOPETROSIS WITH RENAL TUBULAR ACIDOSIS 259750 : OSTEOPOROSIS, JUVENILE #259770 : OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME; OPPG 259775 : OSTEOSCLEROTIC BONE DYSPLASIA, LETHAL *259780 : OTOONYCHOPERONEAL SYNDROME #259900 : HYPEROXALURIA, PRIMARY, TYPE I #260000 : HYPEROXALURIA, PRIMARY, TYPE II *260005 : 5-@OXOPROLINASE DEFICIENCY 260100 : PA POLYMORPHISM OF ALPHA-2-GLOBULIN 260130 : PACHYONYCHIA CONGENITA, RECESSIVE 260150 : PALANT CLEFT PALATE SYNDROME 260200 : PALLIDAL DEGENERATION, PROGRESSIVE, WITH RETINITIS PIGMENTOSA *260300 : PALLIDOPYRAMIDAL SYNDROME #260350 : PANCREATIC CARCINOMA #260370 : PANCREATIC AGENESIS, CONGENITAL *260400 : SHWACHMAN-DIAMOND SYNDROME; SDS 260450 : PANCREATIC INSUFFICIENCY, COMBINED EXOCRINE 260470 : PANENCEPHALITIS, SUBACUTE SCLEROSING 260480 : PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX ^260490 : MOVED TO 174800 260500 : PAPILLOMA OF CHOROID PLEXUS 260530 : PARANA HARD-SKIN SYNDROME 260540 : PARKINSON-DEMENTIA SYNDROME 260555 : PARTINGTON-ANDERSON SYNDROME *260565 : PEHO SYNDROME 260570 : PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN *260600 : PELIZAEUS-MERZBACHER DISEASE, ACUTE INFANTILE TYPE 260650 : PELLAGRA-LIKE SYNDROME 260660 : PELVISCAPULAR DYSPLASIA *260800 : PENTOSURIA 260900 : PERICARDIAL EFFUSION, CHRONIC 260910 : PERIFOLLICULITIS CAPITIS ABSCEDENS ET SUFFODIENS, FAMILIAL #260920 : HYPER-IgD SYNDROME; HIDS 260950 : PERIODONTOSIS, JUVENILE 260970 : PERIPHERAL NEUROPATHY, ATAXIA, FOCAL NECROTIZING ENCEPHALOPATHY, AND SPONGY DEGENERATION OF BRAIN ^260980 : MOVED TO 300388 *261000 : PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR #261100 : MEGALOBLASTIC ANEMIA 1; MGA1 261400 : PERONEUS TERTIUS MUSCLE, ABSENCE OF #261500 : PEROXIDASE AND PHOSPHOLIPID DEFICIENCY IN EOSINOPHILS ^261510 : MOVED TO 261515 *261515 : D-BIFUNCTIONAL PROTEIN DEFICIENCY *261540 : PETERS ANOMALY WITH SHORT-LIMB DWARFISM #261550 : PERSISTENT MULLERIAN DUCT SYNDROME, TYPES I AND II; PMDS 261560 : PFEIFFER-PALM-TELLER SYNDROME 261575 : PHAVER SYNDROME 261590 : PHENFORMIN 4-HYDROXYLATION *261600 : PHENYLKETONURIA *261630 : PHENYLKETONURIA II *261640 : 6-@PYRUVOYLTETRAHYDROPTERIN SYNTHASE; PTS *261650 : PHOSPHOENOLPYRUVATE CARBOXYKINASE 2, MITOCHONDRIAL; PCK2 ^261660 : REMOVED FROM DATABASE *261670 : PHOSPHOGLYCERATE MUTASE, DEFICIENCY OF M SUBUNIT OF *261680 : PHOSPHOENOLPYRUVATE CARBOXYKINASE 1, SOLUBLE; PCK1 261740 : PHOSPHORYLASE KINASE DEFICIENCY OF HEART #261750 : PHOSPHORYLASE KINASE DEFICIENCY OF LIVER AND MUSCLE, AUTOSOMAL RECESSIVE 261800 : PIERRE ROBIN SYNDROME 261900 : PILI TORTI 261990 : PILI TORTI AND DEVELOPMENTAL DELAY *262000 : PILI TORTI AND NERVE DEAFNESS 262020 : PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS #262190 : PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES #262300 : ACHROMATOPSIA 3; ACHM3 #262350 : PITT SYNDROME #262400 : PITUITARY DWARFISM I #262500 : PITUITARY DWARFISM II #262600 : PITUITARY DWARFISM III #262650 : PITUITARY DWARFISM IV 262700 : PITUITARY DWARFISM WITH SMALL SELLA TURCICA 262710 : PITUITARY DWARFISM WITH LARGE SELLA TURCICA ^262780 : MOVED TO 107910 262800 : PLASMA CLOT RETRACTION FACTOR, DEFICIENCY OF *262850 : PLASMIN INHIBITOR DEFICIENCY 262875 : PLATELET PROSTACYCLIN RECEPTOR DEFECT 262890 : PLATELET RECEPTOR FOR FACTOR X, DEFICIENCY OF 262900 : PLEOCONIAL MYOPATHY WITH SALT CRAVING #263000 : PNEUMONITIS, DESQUAMATIVE INTERSTITIAL; DIP 263100 : POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS #263200 : POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE; ARPKD *263210 : POLYCYSTIC KIDNEY DISEASE, POTTER TYPE I, WITH MICROBRACHYCEPHALY, HYPERTELORISM, AND BRACHYMELIA 263300 : POLYCYTHEMIA VERA *263400 : ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN 263450 : POLYDACTYLY, POSTAXIAL 263510 : SHORT RIB-POLYDACTYLY SYNDROME, TYPE III *263520 : SHORT RIB-POLYDACTYLY SYNDROME, TYPE II *263530 : SHORT RIB-POLYDACTYLY SYNDROME, TYPE I 263540 : POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES 263550 : POLYMYOCLONUS, INFANTILE 263560 : POLYNEUROPATHY, MIXED, OF EARLY ONSET *263570 : POLYGLUCOSAN BODY DISEASE, ADULT FORM; APBD 263600 : POLYSACCHARIDE, STORAGE OF UNUSUAL 263610 : POLYHYDRAMNIOS, CHRONIC IDIOPATHIC ^263620 : MOVED TO 240300 263630 : POLYSYNDACTYLY WITH CARDIAC MALFORMATION *263650 : POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE #263700 : PORPHYRIA, CONGENITAL ERYTHROPOIETIC *263750 : POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS #263800 : POTASSIUM AND MAGNESIUM DEPLETION 264010 : PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY 264050 : PRENATAL BOWING 264060 : PREPAPILLARY VASCULAR LOOPS #264070 : HYPERPHENYLALANINEMIA WITH PRIMAPTERINURIA *264080 : PROGESTERONE RESISTANCE; PGR *264090 : PROGEROID SYNDROME, NEONATAL 264110 : PROLACTIN DEFICIENCY, ISOLATED 264120 : PROLACTIN DEFICIENCY WITH OBESITY AND ENLARGED TESTES 264140 : PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, AND DEAFNESS 264150 : PSEUDOACHONDROPLASTIC DYSPLASIA II ^264160 : MOVED TO 177170 264180 : PSEUDODIASTROPHIC DYSPLASIA ^264200 : MOVED TO 221900 *264270 : PSEUDOHERMAPHRODITISM, FEMALE, WITH SKELETAL ANOMALIES #264300 : 17-@BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY #264350 : PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1 264420 : FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM ^264450 : REMOVED FROM DATABASE *264470 : PSEUDONEONATAL ADRENOLEUKODYSTROPHY 264475 : PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HAND ANOMALIES 264480 : PSEUDOTRISOMY 13 SYNDROME 264500 : PSEUDOURIDINURIA AND MENTAL DEFECT *264600 : PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH *264700 : PSEUDOVITAMIN D DEFICIENCY RICKETS #264800 : PSEUDOXANTHOMA ELASTICUM, AUTOSOMAL RECESSIVE; PXE 264810 : PSEUDOXANTHOMA ELASTICUM, RECESSIVE TYPE II *264900 : PTA DEFICIENCY *265000 : PTERYGIUM SYNDROME 265050 : PTOSIS OF EYELIDS WITH DIASTASIS RECTI AND HIP DYSPLASIA *265100 : PULMONARY ALVEOLAR MICROLITHIASIS #265120 : PULMONARY ALVEOLAR PROTEINOSIS 265140 : PULMONARY ARTERIOVENOUS FISTULAS 265150 : PULMONARY ATRESIA WITH INTACT VENTRICULAR SEPTUM 265200 : PULMONARY BULLAE CAUSING PNEUMOTHORAX 265300 : PULMONARY CYSTIC LYMPHANGIECTASIS 265380 : PULMONARY HYPERTENSION, FAMILIAL PERSISTENT, OF THE NEWBORN 265400 : PULMONARY HYPERTENSION, PRIMARY 265430 : PULMONARY HYPOPLASIA 265450 : PULMONARY VENOOCCLUSIVE DISEASE 265500 : PULMONIC STENOSIS 265600 : PULMONIC STENOSIS AND CONGENITAL NEPHROSIS #265800 : PYCNODYSOSTOSIS #265850 : PYGMY 265880 : PYKNOACHONDROGENESIS *265900 : PYLE DISEASE *265950 : PYLORIC ATRESIA *266100 : EPILEPSY, PYRIDOXINE-DEPENDENT; EPD #266120 : URIDINE 5-PRIME MONOPHOSPHATE HYDROLASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO #266130 : 5-@OXOPROLINURIA #266140 : PYROPOIKILOCYTOSIS, HEREDITARY; HPP *266150 : PYRUVATE CARBOXYLASE DEFICIENCY *266200 : PYRUVATE KINASE DEFICIENCY OF ERYTHROCYTE *266250 : RADICULONEUROPATHY, FATAL NEONATAL 266255 : RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATION AND HYPOTONIA #266265 : CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc 266270 : RAMON SYNDROME 266280 : RAPADILINO SYNDROME *266300 : HAIR COLOR 2; HCL2 *266350 : RED SKIN PIGMENT ANOMALY OF NEW GUINEA 266400 : REESE RETINAL DYSPLASIA #266500 : REFSUM DISEASE #266510 : REFSUM DISEASE, INFANTILE FORM #266600 : INFLAMMATORY BOWEL DISEASE 1; IBD1 266810 : RENAL AND MULLERIAN DUCT HYPOPLASIA #266900 : SENIOR-LOKEN SYNDROME 266910 : RENAL DYSPLASIA-LIMB DEFECTS SYNDROME 266920 : RENAL DYSPLASIA, RETINAL PIGMENTARY DYSTROPHY, CEREBELLAR ATAXIA, AND SKELETAL DYSPLASIA *267000 : RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM 267010 : RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST 267200 : RENAL TUBULAR ACIDOSIS III #267300 : RENAL TUBULAR ACIDOSIS WITH PROGRESSIVE NERVE DEAFNESS 267400 : RENAL, GENITAL, AND MIDDLE EAR ANOMALIES *267430 : RENAL TUBULAR DYSGENESIS #267450 : RESPIRATORY DISTRESS SYNDROME 267480 : RESPIRATORY UNDERRESPONSIVENESS TO HYPOXIA AND HYPERCAPNIA *267500 : RETICULAR DYSGENESIA #267700 : RETICULOSIS, FAMILIAL HISTIOCYTIC 267730 : RETICULUM CELL SARCOMA 267740 : RETINAL DEGENERATION AND EPILEPSY #267750 : KNOBLOCH SYNDROME; KNO 267760 : RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION, AND ANGLE CLOSURE GLAUCOMA 267800 : RETINAL DYSTROPHY, RETICULAR PIGMENTARY, OF POSTERIOR POLE 267900 : RETINAL TELANGIECTASIA AND HYPOGAMMAGLOBULINEMIA #268000 : RETINITIS PIGMENTOSA; RP 268010 : RETINITIS PIGMENTOSA INVERSA WITH DEAFNESS 268020 : RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM 268025 : RETINITIS PIGMENTOSA, LATE-ADULT ONSET ^268030 : MOVED TO 600105 268040 : RETINOHEPATOENDOCRINOLOGIC SYNDROME 268050 : RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION 268060 : RETINOPATHY, PERICENTRAL PIGMENTARY, RECESSIVE *268080 : RETINOSCHISIS OF FOVEA #268100 : ENHANCED S-CONE SYNDROME; ESCS 268130 : REVESZ SYNDROME #268150 : RH-NULL, REGULATOR TYPE; RHN *268200 : RHABDOMYOLYSIS, ACUTE RECURRENT #268210 : RHABDOMYOSARCOMA 1; RMS1 #268220 : RHABDOMYOSARCOMA 2; RMS2 268240 : RHEUMATIC FEVER-RELATED ANTIGEN 268250 : RHIZOMELIC SYNDROME *268300 : ROBERTS SYNDROME; RBS 268305 : ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES #268310 : ROBINOW SYNDROME, AUTOSOMAL RECESSIVE 268315 : ROD-CONE DYSTROPHY, SENSORINEURAL DEAFNESS, AND FANCONI-TYPE RENAL DYSFUNCTION 268320 : RODRIGUES BLINDNESS #268400 : ROTHMUND-THOMSON SYNDROME; RTS 268500 : ROWLEY-ROSENBERG SYNDROME 268650 : RUDIGER SYNDROME #268670 : RUTLEDGE LETHAL MULTIPLE CONGENITAL ANOMALY SYNDROME *268700 : SACCHAROPINURIA #268800 : SANDHOFF DISEASE 268850 : SAO PAULO MCA/MR SYNDROME 268900 : SARCOSINEMIA 268950 : SARCOTUBULAR MYOPATHY #269000 : SC PHOCOMELIA SYNDROME 269150 : SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME #269160 : SCHIZENCEPHALY 269200 : SCHMIDT SYNDROME *269250 : SCHNECKENBECKEN DYSPLASIA 269300 : SCHWARTZ-LELEK SYNDROME 269400 : SCLEROCORNEA #269500 : SCLEROSTEOSIS; SOST #269600 : SEA-BLUE HISTIOCYTE DISEASE 269630 : SECOND METATARSAL-METACARPAL SYNDROME 269650 : SECRETORY COMPONENT DEFICIENCY #269700 : BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY; BSCL 269720 : SEIZURES, BENIGN FAMILIAL NEONATAL 269800 : SENILE PLAQUE FORMATION 269840 : SEVERE COMBINED IMMUNODEFICIENCY, ATYPICAL *269860 : SHORT RIB-POLYDACTYLY SYNDROME, TYPE IV 269870 : SHORT STATURE-OBESITY SYNDROME; SSOS 269880 : SHORT SYNDROME #269920 : INFANTILE SIALIC ACID STORAGE DISORDER #269921 : SIALURIA 269950 : SIDEROBLASTIC ANEMIA, AUTOSOMAL ^270050 : MOVED TO 180860 *270100 : SITUS INVERSUS VISCERUM 270150 : SJOGREN SYNDROME *270200 : SJOGREN-LARSSON SYNDROME 270220 : SJOGREN-LARSSON-LIKE ICHTHYOSIS WITHOUT CNS OR EYE INVOLVEMENT 270230 : SKELETAL DYSPLASIA, SAN DIEGO TYPE 270240 : SKELETAL DYSPLASIA WITH TELANGIECTASES AND MESODERMAL DYSGENESIS OF THE IRIS *270300 : SKIN PEELING, FAMILIAL CONTINUOUS 270350 : SKUNK N-BUTYLMERCAPTAN, INABILITY TO SMELL #270400 : SMITH-LEMLI-OPITZ SYNDROME; SLOS 270420 : SODIUM DIARRHEA, CONGENITAL 270425 : SODIUM-POTASSIUM-ATPase ACTIVITY OF RED CELL 270450 : SOMATOMEDIN, END-ORGAN INSENSITIVITY TO 270460 : SONODA SYNDROME 270500 : SPASTIC ATAXIA #270550 : SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE; SACS *270600 : SPASTIC DIPLEGIA, INFANTILE TYPE 270680 : SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES *270685 : SPASTIC PARAPLEGIA 17 *270700 : SPASTIC PARAPLEGIA AND RETINAL DEGENERATION 270710 : FITZSIMMONS-GUILBERT SYNDROME 270750 : SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES *270800 : SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A 270805 : SPASTIC PARAPLEGIA WITH MYOCLONIC EPILEPSY 270850 : SPASTIC PARESIS, GLAUCOMA, AND MENTAL RETARDATION 270900 : SPASTIC PSEUDOSCLEROSIS 270950 : SPASTIC QUADRIPLEGIA, RETINITIS PIGMENTOSA, AND MENTAL RETARDATION 270960 : SPERMATOGENESIS ARREST #270970 : SPHEROCYTOSIS, AUTOSOMAL RECESSIVE 271100 : SPINAL EXTRADURAL CYST 271109 : SPINAL MUSCULAR ATROPHY WITH MENTAL RETARDATION 271110 : SPINAL MUSCULAR ATROPHY WITH MICROCEPHALY AND MENTAL SUBNORMALITY ^271120 : MOVED TO 182960 271150 : SPINAL MUSCULAR ATROPHY, PROXIMAL, ADULT TYPE 271200 : SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE 271220 : SPINAL MUSCULAR ATROPHY, SCAPULOPERONEAL 271225 : SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES *271245 : INFANTILE-ONSET SPINOCEREBELLAR ATAXIA; IOSCA *271250 : SPINOCEREBELLAR ATAXIA WITH BLINDNESS AND DEAFNESS 271270 : SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM 271310 : SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY 271320 : SPINOCEREBELLAR DEGENERATION WITH MACULAR CORNEAL DYSTROPHY, CONGENITAL CATARACTS, AND MYOPIA 271322 : SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM *271400 : SPLENIC HYPOPLASIA 271500 : SPLENOPORTAL VASCULAR ANOMALIES 271510 : SPONASTRIME DYSPLASIA 271520 : SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES 271530 : SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA *271550 : SPONDYLOENCHONDRODYSPLASIA *271600 : SPONDYLOEPIPHYSEAL DYSPLASIA TARDA 271620 : SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH MENTAL RETARDATION *271630 : SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE *271640 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY; SEMDJL *271650 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE; SEMDIT 271665 : SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE 271700 : SPONDYLOPERIPHERAL DYSPLASIA WITH SHORT ULNA *271900 : CANAVAN DISEASE 271930 : STRIATONIGRAL DEGENERATION, INFANTILE 271950 : SUBAORTIC STENOSIS, MEMBRANOUS 271960 : SUBAORTIC STENOSIS--SHORT STATURE SYNDROME *271980 : ALDEHYDE DEHYDROGENASE 5 FAMILY, MEMBER A1; ALDH5A1 272000 : SUCROSURIA, HIATUS HERNIA AND MENTAL RETARDATION 272100 : SUDANOPHILIC CEREBRAL SCLEROSIS #272120 : SUDDEN INFANT DEATH SYNDROME 272150 : SUGARMAN BRACHYDACTYLY *272200 : MULTIPLE SULFATASE DEFICIENCY #272300 : SULFOCYSTEINURIA 272350 : SUMMITT SYNDROME *272370 : SUSCEPTIBILITY TO LYSIS BY ALLOREACTIVE NATURAL KILLER CELLS; EC1 272430 : SWEATING, COLD-INDUCED 272440 : SYNDACTYLY, TYPE I, WITH MICROCEPHALY AND MENTAL RETARDATION 272450 : SYNDESMODYSPLASIC DWARFISM *272460 : SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME 272480 : SYRINGOMYELIA 272500 : SYSTEMIC CYSTIC ANGIOMATOSIS AND SEIP SYNDROME 272550 : TACHYCARDIA, HYPERTENSION, MICROPHTHALMOS, AND HYPERGLYCINURIA 272600 : TAPETORETINAL DEGENERATION WITH ATAXIA 272620 : TARDIVE DYSKINESIA *272650 : TATSUMI FACTOR DEFICIENCY 272700 : TAURODONTISM *272750 : TAY-SACHS DISEASE, AB VARIANT #272800 : TAY-SACHS DISEASE; TSD 272950 : TEEBI-SHALTOUT SYNDROME 272980 : TEETH, CONGENITAL ABSENCE OF, WITH TAURODONTIA AND SPARSE HAIR 273000 : TEETH, FUSED 273050 : TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM 273120 : TERATOMA, PINEAL 273150 : TESTES, RUDIMENTARY 273250 : TESTICULAR REGRESSION SYNDROME; TRS *273300 : TESTICULAR TUMORS ^273350 : MOVED TO 154230 273390 : TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES *273395 : TETRA-AMELIA WITH PULMONARY HYPOPLASIA 273400 : TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, AND OTHER ABNORMALITIES 273490 : THALAMIC DEGENERATION, SYMMETRIC INFANTILE 273600 : THALIDOMIDE SUSCEPTIBILITY 273680 : THANATOPHORIC DYSPLASIA, GLASGOW VARIANT 273730 : THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME 273740 : THORACOMELIC DYSPLASIA *273750 : THREE M SYNDROME 273770 : THREONINEMIA *273800 : THROMBASTHENIA OF GLANZMANN AND NAEGELI *273900 : THROMBOCYTOPENIA, AUTOSOMAL RECESSIVE *274000 : THROMBOCYTOPENIA--ABSENT RADIUS SYNDROME #274150 : THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL *274180 : THROMBOXANE A SYNTHASE 1; TBXAS1 *274190 : THUMB AGENESIS, SHORT STATURE, AND IMMUNODEFICIENCY 274200 : THUMB, DISTAL HYPEREXTENSIBILITY OF 274205 : THUMB, HYPOPLASTIC, WITH CHOROID COLOBOMA, POORLY DEVELOPED ANTIHELIX, AND DEAFNESS 274210 : THYMIC APLASIA WITH FETAL DEATH 274230 : THYMOMA, FAMILIAL 274240 : THYROCEREBRORETINAL SYNDROME 274260 : THYMIC NEOPLASIA 274265 : THYMIC-RENAL-ANAL-LUNG DYSPLASIA *274270 : DIHYDROPYRIMIDINE DEHYDROGENASE; DPYD #274300 : THYROID HORMONE UNRESPONSIVENESS #274400 : THYROID HORMONOGENESIS, GENETIC DEFECT IN, I #274500 : THYROID HORMONE ORGANIFICATION DEFECT II #274600 : PENDRED SYNDROME; PDS *274700 : THYROID HORMONOGENESIS, GENETIC DEFECT IN, III *274800 : THYROID HORMONOGENESIS, GENETIC DEFECT IN, IV 274900 : THYROID HORMONOGENESIS, GENETIC DEFECT IN, V #275000 : GRAVES DISEASE #275100 : THYROTROPIN DEFICIENCY, ISOLATED *275120 : THYROTROPIN-RELEASING HORMONE DEFICIENCY 275190 : TIGLICACIDEMIA #275200 : THYROTROPIN, UNRESPONSIVENESS TO *275210 : TIGHT SKIN CONTRACTURE SYNDROME, LETHAL 275220 : TIBIAL HEMIMELIA 275230 : TIBIA, ABSENCE OF, WITH CONGENITAL DEAFNESS 275240 : TINEA IMBRICATA, SUSCEPTIBILITY TO *275250 : TONGUE, PIGMENTED FUNGIFORM PAPILLAE OF 275300 : TRACHEOBRONCHOMEGALY *275350 : TRANSCOBALAMIN II DEFICIENCY *275355 : TRANSFORMING GROWTH FACTOR, BETA-1 RESPONSE ELEMENT *275360 : TREHALASE; TREH *275370 : TRICARBOXYLIC ACID CYCLE, DEFECT OF 275400 : TRICHOMEGALY WITH MENTAL RETARDATION, DWARFISM, AND PIGMENTARY DEGENERATION OF RETINA 275450 : TRICHOODONTOONYCHIAL DYSPLASIA ^275500 : MOVED TO 190350 275550 : TRICHORRHEXIS NODOSA SYNDROME 275595 : TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIES OF THE HANDS AND FEET 275600 : TRIGONOCEPHALY #275630 : TRIGLYCERIDE STORAGE DISEASE WITH IMPAIRED LONG-CHAIN FATTY ACID OXIDATION ^275650 : MOVED TO 214950 *275900 : TROYER SYNDROME *276000 : PROTEASE, SERINE, 1; PRSS1 *276100 : TRYPTOPHANURIA WITH DWARFISM 276200 : T-SUBSTANCE ANOMALY #276300 : TURCOT SYNDROME *276400 : TWINNING, DIZYGOTIC 276410 : TWINNING, MONOZYGOTIC 276500 : TYROSINE METABOLISM, DELAYED MATURATION IN *276600 : TYROSINE TRANSAMINASE DEFICIENCY *276700 : TYROSINEMIA, TYPE I *276710 : TYROSINEMIA, TYPE III 276800 : TYROSINOSIS *276820 : ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY 276821 : ULNAR HYPOPLASIA WITH MENTAL RETARDATION 276822 : ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS #276850 : SCHULMAN-UPSHAW SYNDROME; USS 276880 : UROCANASE DEFICIENCY *276900 : USHER SYNDROME, TYPE IA; USH1A *276901 : USHER SYNDROME, TYPE IIA; USH2A #276902 : USHER SYNDROME, TYPE III; USH3 *276903 : MYOSIN VIIA; MYO7A #276904 : USHER SYNDROME, TYPE IC; USH1C *276905 : USHER SYNDROME, TYPE IIB; USH2B 276950 : VACTERL ASSOCIATION WITH HYDROCEPHALUS 277000 : VAGINA, ABSENCE OF *277100 : VALINEMIA *277150 : VAN BOGAERT-HOZAY SYNDROME *277170 : VARADI-PAPP SYNDROME 277175 : VASCULAR HYALINOSIS #277180 : VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD 277200 : RIGHT VENTRICULAR HYPOPLASIA, ISOLATED #277300 : SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE, 1 *277320 : VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA *277350 : VITAMIN A METABOLIC DEFECT 277380 : VITAMIN B12 LYSOSOMAL RELEASE DEFECT *277400 : VITAMIN B12 METABOLIC DEFECT WITH METHYLMALONICACIDEMIA AND HOMOCYSTINURIA *277410 : VITAMIN B12 METABOLIC DEFECT, TYPE 2 277420 : VITAMIN D-DEPENDENT RICKETS, TYPE II #277440 : VITAMIN D-RESISTANT RICKETS WITH END-ORGAN UNRESPONSIVENESS TO 1,25-DIHYDROXYCHOLECALCIFEROL #277450 : VITAMIN K-DEPENDENT COAGULATION DEFECT #277460 : VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF; VED 277465 : VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION *277470 : VOLENDAM NEURODEGENERATIVE DISEASE #277480 : VON WILLEBRAND DISEASE, RECESSIVE FORM #277580 : WAARDENBURG-SHAH SYNDROME 277590 : WEAVER SYNDROME *277600 : WEILL-MARCHESANI SYNDROME #277610 : WEISSENBACHER-ZWEYMULLER SYNDROME; WZS #277700 : WERNER SYNDROME; WRN 277720 : WHISTLING FACE SYNDROME, RECESSIVE FORM *277730 : WERNICKE-KORSAKOFF SYNDROME 277740 : WHITE FORELOCK WITH MALFORMATIONS #277900 : WILSON DISEASE *277950 : WINCHESTER DISEASE 277970 : WISKOTT-ALDRICH SYNDROME 277990 : WOLFF MENTAL RETARDATION SYNDROME *278000 : WOLMAN DISEASE 278100 : WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS 278150 : WOOLLY HAIR, AUTOSOMAL RECESSIVE 278200 : WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS ^278205 : MOVED TO 601214 *278250 : WRINKLY SKIN SYNDROME; WSS *278300 : XANTHINURIA, TYPE I #278400 : RUFOUS OCULOCUTANEOUS ALBINISM; ROCA ^278600 : MOVED TO 236800 *278700 : XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA *278720 : XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC #278730 : XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD *278740 : XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E #278750 : XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES #278760 : XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF #278780 : XERODERMA PIGMENTOSUM VII #278800 : DE SANCTIS-CACCHIONE SYNDROME 278810 : XERODERMA PIGMENTOSUM IX 278850 : XX MALE SYNDROME 278900 : XYLOSIDASE DEFICIENCY 279000 : YOUNG SYNDROME 280000 : ZUNICH NEUROECTODERMAL SYNDROME *300000 : OPITZ SYNDROME *300001 : ICHTHYOSIS, X-LINKED, WITHOUT STEROID SULFATASE DEFICIENCY *300002 : ARYLSULFATASE D; ARSD *300003 : ARYLSULFATASE F; ARSF 300004 : CORPUS CALLOSUM, AGENESIS OF, WITH SEIZURES AND MICRENCEPHALY *300005 : METHYL-CpG-BINDING PROTEIN 2; MECP2 *300006 : CALTRACTIN; CALT *300007 : INTERLEUKIN 9 RECEPTOR; IL9R *300008 : CHLORIDE CHANNEL 5; CLCN5 #300009 : DENT DISEASE *300010 : A-11 GENE; A11 *300011 : ATPase, Cu(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A *300012 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY A, MEMBER 1; SMARCA1 *300013 : N-ACETYLTRANSFERASE ARD1, S. CEREVISIAE, HOMOLOG OF; DXS707 *300014 : ATPase, Ca(2+)-TRANSPORTING, PLASMA MEMBRANE, 3; ATP2B3 *300015 : ACETYLSEROTONIN METHYLTRANSFERASE, X-CHROMOSOMAL; ASMT *300016 : MELANOMA ANTIGEN, FAMILY A, 1; MAGEA1 *300017 : FILAMIN A; FLNA #300018 : DOSAGE-SENSITIVE SEX REVERSAL; DSS *300019 : HOST CELL FACTOR C1; HCFC1 *300020 : ACTIN-LIKE 1; ACTL1 *300021 : SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE *300022 : PLEXIN A3; PLXNA3 *300023 : GTPase-ACTIVATING PROTEIN, RHO, 4; ARHGAP4 *300024 : ZINC FINGER PROTEIN 157; ZNF157 *300025 : CAUDAL-TYPE HOMEO BOX TRANSCRIPTION FACTOR 4; CDX4 *300026 : NUCLEOSOME ASSEMBLY PROTEIN 1-LIKE 2; NAP1L2 *300027 : RNA-BINDING MOTIF PROTEIN 3; RBM3 *300028 : U2 SMALL NUCLEAR RIBONUCLEOPROTEIN AUXILIARY FACTOR, SMALL SUBUNIT 2 #300029 : RETINITIS PIGMENTOSA 15; RP15 *300030 : DEAFNESS, X-LINKED 4, CONGENITAL SENSORINEURAL; DFN4 *300031 : FRAGILE SITE F, X-LINKED; FRAXF *300032 : ATR-X GENE; ATRX *300033 : MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 7; MLLT7 *300034 : ANGIOTENSIN II RECEPTOR, TYPE 2; AGTR2 *300035 : EPHRIN B1; EFNB1 *300036 : SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, CREATINE), MEMBER 8; SLC6A8 *300037 : GLYPICAN 3; GPC3 *300038 : PYRIMIDINERGIC RECEPTOR P2Y, G PROTEIN-COUPLED, 4; P2RY4 *300039 : POU DOMAIN, CLASS 3, TRANSCRIPTION FACTOR 4; POU3F4 *300040 : SMC1-LIKE 1; SMC1L1 *300041 : GUANYLYL CYCLASE 2F, RETINAL; GUCY2F 300042 : ALOPECIA, CONGENITAL *300043 : HEPATOMA-DERIVED GROWTH FACTOR; HDGF *300044 : TRANSKETOLASE-LIKE 1; TKTL1 ^300045 : MOVED TO 602081 *300046 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, 23; MRX23 *300047 : MENTAL RETARDATION, X-LINKED 20; MRX20 *300048 : INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED #300049 : HETEROTOPIA, PERIVENTRICULAR *300050 : UBIQUITIN-SPECIFIC PROTEASE 11; USP11 *300051 : GLYCOPROTEIN M6B; GPM6B *300052 : DYSTROPHIN-RELATED PROTEIN 2; DRP2 *300053 : SYNAPTOBREVIN-LIKE 1; SYBL1 300054 : BODY LENGTH, MOUSE, HUMAN HOMOLOG #300055 : MENTAL RETARDATION WITH PSYCHOSIS, PYRAMIDAL SIGNS, AND MACROORCHIDISM *300056 : HOLOCYTOCHROME C SYNTHASE; HCCS ^300057 : MOVED TO 601324 300058 : PEM HOMEO BOX GENE, HUMAN HOMOLOG OF *300059 : CHROMOSOME X OPEN READING FRAME 12; CXORF12 *300060 : DXS9879E *300061 : ZINC FINGER PROTEIN 261; ZNF261 300062 : MENTAL RETARDATION, X-LINKED 14; MRX14 ^300063 : MOVED TO 304930 300064 : MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM *300065 : FSH PRIMARY RESPONSE, RAT, HOMOLOG 1; FSHPRH1 *300066 : DEAFNESS, X-LINKED 6, PROGRESSIVE; DFN6 #300067 : LISSENCEPHALY, X-LINKED #300068 : ANDROGEN INSENSITIVITY SYNDROME; AIS #300069 : CARDIOMYOPATHY, DILATED, 3A; CMD3A *300070 : FIBROBLAST GROWTH FACTOR 13; FGF13 #300071 : NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2; CSNB2 *300072 : UBIQUITIN-SPECIFIC PROTEASE 9, X CHROMOSOME; USP9X 300073 : FETAL AKINESIA SYNDROME, X-LINKED 300074 : X CHROMOSOME-CONTROLLING ELEMENT Xce, MOUSE, HOMOLOG OF *300075 : RIBOSOMAL PROTEIN S6 KINASE, 90-KD, 3; RPS6KA3 *300076 : IMMUNONEUROLOGIC DISORDER, X-LINKED *300077 : MENTAL RETARDATION, X-LINKED 29; MRX29 *300078 : NADH-UBIQUINONE OXIDOREDUCTASE 1 ALPHA SUBCOMPLEX, 1; NDUFA1 *300079 : BACULOVIRAL IAP REPEAT-CONTAINING PROTEIN 4; BIRC4 *300080 : RNA-BINDING MOTIF PROTEIN 10; RBM10 *300081 : DEOXYRIBONUCLEASE I-LIKE 1; DNASE1L1 *300082 : COGNITIVE FUNCTION 1, SOCIAL; CGF1 *300083 : PROTEIN KINASE, X-LINKED; PRKX *300084 : NON-POU DOMAIN-CONTAINING OCTAMER-BINDING PROTEIN; NONO *300085 : CONE DYSTROPHY, X-LINKED, 2; COD2 *300086 : G PROTEIN-COUPLED RECEPTOR 23; GPR23 #300087 : X INACTIVATION, FAMILIAL SKEWED, 1; SXI1 *300088 : EPILEPSY, FEMALE RESTRICTED, WITH MENTAL RETARDATION; EFMR *300089 : ISOCITRATE DEHYDROGENASE 3, GAMMA SUBUNIT; IDH3G *300090 : SIGNAL SEQUENCE RECEPTOR, DELTA; SSR4 *300091 : FOS-INDUCED GROWTH FACTOR; FIGF *300092 : CHROMOSOME X OPEN READING FRAME 2; CXORF2 *300093 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, EPSILON; GABRE *300094 : PROTEIN KINASE C, IOTA FORM; PRKCI *300095 : SOLUTE CARRIER FAMILY 16, MEMBER 2; SLC16A2 *300096 : TRANSMEMBRANE 4 SUPERFAMILY, MEMBER 2; TM4SF2 *300097 : MELANOMA ANTIGEN, FAMILY B, 1; MAGEB1 *300098 : MELANOMA ANTIGEN, FAMILY B, 2; MAGEB2 ^300099 : MOVED TO 300097 *300100 : ADRENOLEUKODYSTROPHY; ALD *300101 : BONE MARROW KINASE, X-LINKED; BMX *300102 : GS2 GENE; DXS1283E *300103 : APICAL PROTEIN OF XENOPUS-LIKE; APXL *300104 : GDP DISSOCIATION INHIBITOR 1; GDI1 *300105 : SPERMINE SYNTHASE; SMS 300106 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED *300107 : BOMBESIN-LIKE RECEPTOR 3; BRS3 *300108 : DIAPHANOUS, DROSOPHILA, HOMOLOG OF, 2; DIAPH2 *300109 : PROTEIN PHOSPHATASE, EF-HAND CALCIUM-BINDING DOMAIN 1; PPEF1 *300110 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, ALPHA-1F SUBUNIT; CACNA1F *300111 : LIM DOMAIN ONLY 6; LMO6 *300112 : PROTEOLIPID PROTEIN 2; PLP2 *300113 : X-LINKED B CELL SURFACE ANTIGEN, MOUSE, HOMOLOG-LIKE 1; XLRL *300114 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 49; MRX49 *300115 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 50; MRX50 *300116 : MATURE T-CELL PROLIFERATION 1; MTCP1 *300117 : NUCLEOSOME ASSEMBLY PROTEIN 1-LIKE 3; NAP1L3 *300118 : GTPase-ACTIVATING PROTEIN, RHO, 6; ARHGAP6 *300119 : INTERLEUKIN 13 RECEPTOR, ALPHA-1; IL13RA1 *300120 : CHROMOSOME X OPEN READING FRAME 6; CXORF6 *300121 : DOUBLECORTIN; DCX ^300122 : MOVED TO 300000 *300123 : MENTAL RETARDATION, X-LINKED, WITH ISOLATED GROWTH HORMONE DEFICIENCY; MRGH *300124 : PSEUDOAUTOSOMAL GTP-BINDING PROTEIN-LIKE *300125 : MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO *300126 : DYSKERIN; DKC1 *300127 : OLIGOPHRENIN 1; OPHN1 *300128 : UBIQUITOUSLY TRANSCRIBED TETRATRICOPEPTIDE REPEAT GENE ON X CHROMOSOME; UTX 300129 : HEMATOPOIETIC STEM CELL KINETICS, CONTROL OF *300130 : INTERLEUKIN 13 RECEPTOR, ALPHA-2; IL13RA2 *300131 : PLASTIN 3; PLS3 *300132 : TROPHININ; TRO *300133 : VON HIPPEL-LINDAU BINDING PROTEIN 1; VBP1 *300134 : DUAL-SPECIFICITY PHOSPHATASE 9; DUSP9 *300135 : ATP-BINDING CASSETTE, SUBFAMILY B, MEMBER 7; ABCB7 *300136 : DIABETES MELLITUS, INSULIN-DEPENDENT, X-LINKED, SUSCEPTIBILITY TO *300137 : IMMUNOGLOBULIN SUPERFAMILY, MEMBER 1; IGSF1 *300138 : CHLORIDE INTRACELLULAR CHANNEL 2; CLIC2 *300139 : IMMUNOGLOBULIN-BINDING PROTEIN 1; IGBP1 *300140 : EUKARYOTIC TRANSLATION ELONGATION FACTOR 1, BETA-4; EEF1B4 *300141 : PROTEIN PHOSPHATASE 6, CATALYTIC SUBUNIT; PPP6C *300142 : p21-ACTIVATED KINASE 3; PAK3 ^300143 : MOVED TO 309530 *300144 : GLUTAMATE DEHYDROGENASE 2 *300145 : X-PROLYL AMINOPEPTIDASE 2; XPNPEP2 *300146 : CALPAIN 6; CAPN6 *300147 : PROSTATE CANCER, HEREDITARY, X-LINKED; HPCX *300148 : MENTAL RETARDATION, EPILEPTIC SEIZURES, HYPOGONADISM AND HYPOGENITALISM, MICROCEPHALY, AND OBESITY; MEHMO *300149 : CBP/p300-INTERACTING TRANSACTIVATOR WITH GLU/ASP-RICH C-TERMINAL DOMAIN, 1; CITED1 *300150 : SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER), MEMBER A5; SLC25A5 *300151 : SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER), MEMBER A6; SLC25A6 *300152 : MELANOMA ANTIGEN, FAMILY B, 3; MAGEB3 *300153 : MELANOMA ANTIGEN, FAMILY B, 4; MAGEB4 300154 : EXTRAEMBRYONIC, SPERMATOGENESIS, HOMEO BOX 1, MOUSE, HOMOLOG OF *300155 : RETINITIS PIGMENTOSA 24; RP24 *300156 : CANCER/TESTIS ANTIGEN 1; CTAG1 *300157 : FATTY ACID CoA LIGASE, LONG-CHAIN 4; FACL4 *300158 : ARTHROGRYPOSIS, X-LINKED, TYPE V; AMCX5 *300159 : THYMOSIN, BETA-4, X CHROMOSOME; TMSB4X *300160 : DEAD/H BOX 3, X-LINKED; DDX3 *300161 : EUKARYOTIC TRANSLATION INITIATION FACTOR 2, SUBUNIT 3; EIF2S3 *300162 : ACETYLSEROTONIN METHYLTRANSFERASE-LIKE; ASMTL *300163 : FOUR-AND-A-HALF LIM DOMAINS 1; FHL1 *300164 : INACTIVATION ESCAPE 1; INE1 *300165 : INACTIVATION ESCAPE 2; INE2 300166 : OCULOFACIOCARDIODENTAL SYNDROME *300167 : HEPHAESTIN; HEPH *300168 : GLYPICAN 4; GPC4 *300169 : PROGRAMMED CELL DEATH 8; PDCD8 *300170 : CHROMOSOME X OPEN READING FRAME 5; CXORF5 *300171 : MYOTUBULARIN-RELATED PROTEIN 1; MTMR1 *300172 : CALCIUM/CALMODULIN-DEPENDENT SERINE PROTEIN KINASE; CASK *300173 : MELANOMA ANTIGEN, FAMILY A, 2; MAGEA2 *300174 : MELANOMA ANTIGEN, FAMILY A, 3; MAGEA3 *300175 : MELANOMA ANTIGEN, FAMILY A, 4; MAGEA4 *300176 : MELANOMA ANTIGEN, FAMILY A, 6; MAGEA6 *300177 : MELANOMA ANTIGEN, FAMILY A, 12; MAGEA12 *300178 : AC-LIKE TRANSPOSABLE ELEMENT; ALTE *300179 : X INACTIVATION, FAMILIAL SKEWED, 2 *300180 : ARYLSULFATASE E; ARSE *300181 : X INACTIVATION-SPECIFIC TRANSCRIPT-ANTISENSE; TSIX *300182 : COFACTOR REQUIRED FOR SP1 TRANSCRIPTIONAL ACTIVATION, SUBUNIT 2; CRSP2 #300183 : NONCOMPACTION OF LEFT VENTRICULAR MYOCARDIUM, FAMILIAL ISOLATED; INVM 300184 : HYPOTONIA, CONGENITAL NYSTAGMUS, ATAXIA, AND ABNORMAL AUDITORY BRAIN STEM RESPONSES *300185 : A-KINASE ANCHOR PROTEIN 4; AKAP4 *300186 : EUKARYOTIC TRANSLATION INITIATION FACTOR 1A; EIF1A *300187 : SUSHI REPEAT-CONTAINING PROTEIN, X CHROMOSOME; SRPX *300188 : TRINUCLEOTIDE REPEAT-CONTAINING GENE 11; TNRC11 *300189 : DISCS LARGE, DROSOPHILA, HOMOLOG OF, 3; DLG3 *300190 : SH3-BINDING DOMAIN AND GLUTAMIC ACID-RICH PROTEIN-LIKE PROTEIN; SH3BGRL *300191 : TRANSMEMBRANE 4 SUPERFAMILY, MEMBER 6; TM4SF6 *300192 : SARCOMA, SYNOVIAL, X BREAKPOINT 2; SSX2 *300193 : HIGH MOBILITY GROUP PROTEIN 4; HMG4 #300194 : AMME COMPLEX *300195 : ALPORT SYNDROME, MENTAL RETARDATION, MIDFACE HYPOPLASIA, AND ELLIPTOCYTOSIS CHROMOSOMAL REGION GENE 1; AMMECR1 *300196 : TRANSDUCIN-BETA-LIKE 1, X-LINKED; TBL1X *300197 : ATPase, H+ TRANSPORTING, LYSOSOMAL, SUBUNIT 1; ATP6S1 *300198 : GLYCOGENIN 2; GYG2 *300199 : RNA-BINDING MOTIF PROTEIN, X CHROMOSOME; RBMX *300200 : ADRENAL HYPOPLASIA, CONGENITAL; AHC *300201 : CYSTEINYL LEUKOTRIENE RECEPTOR 1 *300202 : SEDLIN; SEDL *300203 : SERINE/THREONINE PROTEIN KINASE 9; STK9 *300204 : MIDLINE 2 *300205 : EMOPAMIL-BINDING PROTEIN; EBP *300206 : INTERLEUKIN 1 RECEPTOR ACCESSORY PROTEIN-LIKE 1; IL1RAPL1 *300207 : G PROTEIN-COUPLED RECEPTOR 50; GPR50 *300208 : SEX COMB ON MIDLEG, DROSOPHILA, HOMOLOG-LIKE 2; SCML2 *300209 : SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 *300210 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, 58; MRX58 *300211 : EPISODIC MUSCLE WEAKNESS, X-LINKED; EMWX *300212 : REGUCALCIN; RGN *300213 : CAAX BOX PROTEIN 1; CXX1 *300214 : PLEXIN B3; PLXNB3 300215 : LISSENCEPHALY, X-LINKED, WITH AMBIGUOUS GENITALIA #300216 : COATS DISEASE *300217 : RETINOIC ACID-INDUCED 2; RAI2 *300218 : MENTAL RETARDATION, X-LINKED, SYNDROMIC 7; MRXS7 #300219 : MYOTUBULAR MYOPATHY WITH ABNORMAL GENITAL DEVELOPMENT *300220 : CHORIOATHETOSIS WITH MENTAL RETARDATION AND ABNORMAL BEHAVIOR *300221 : HODGKIN DISEASE, X-LINKED PSEUDOAUTOSOMAL *300222 : INTEGRAL MEMBRANE PROTEIN 2A; ITM2A *300223 : MELANOMA ANTIGEN, FAMILY C, 1; MAGEC1 *300224 : MELANOMA ANTIGEN, FAMILY D, 1; MAGED1 *300225 : NADPH OXIDASE 1; NOX1 *300226 : SMALL MUSCLE PROTEIN, X-LINKED; SMPX *300227 : SEX COMB ON MIDLEG, DROSOPHILA, HOMOLOG-LIKE 1; SCML1 *300228 : TESTICULAR GERM CELL TUMOR 1 *300229 : VARIABLY CHARGED, X CHROMOSOME; VCX *300230 : CARBONIC ANHYDRASE VB, MITOCHONDRIAL; CA5B *300231 : SOLUTE CARRIER FAMILY 9, ISOFORM A6; SLC9A6 300232 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION 300233 : RADIOULNAR SYNOSTOSIS, RADIAL RAY ABNORMALITIES, AND SEVERE MALFORMATIONS IN THE MALE *300234 : UBIQUITOUSLY EXPRESSED TRANSCRIPT; UXT *300235 : ZINC FINGER-ENCODING GENE, X-LINKED, DUPLICATED, A; ZXDA *300236 : ZINC FINGER-ENCODING GENE, X-LINKED, DUPLICATED, B; ZXDB *300237 : TRANSCRIPTION ELONGATION FACTOR A-LIKE 1; TCEAL1 *300238 : MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11 *300239 : EPIDERMAL GROWTH FACTOR-LIKE 6; EGFL6 #300240 : HOYERAAL-HREIDARSSON SYNDROME; HHS *300241 : G PROTEIN-COUPLED RECEPTOR 34; GPR34 *300242 : SOLUTE CARRIER FAMILY 25, MEMBER 14; SLC25A14 *300243 : MENTAL RETARDATION, X-LINKED, SOUTH AFRICAN TYPE *300244 : TERMINAL OSSEOUS DYSPLASIA AND PIGMENTARY DEFECTS *300245 : PTOSIS, HEREDITARY CONGENITAL 2 *300246 : PROTOCADHERIN 11, X-LINKED; PCDH11X *300247 : BONE MORPHOGENETIC PROTEIN 15; BMP15 *300248 : INHIBITOR OF KAPPA LIGHT POLYPEPTIDE GENE ENHANCER IN B CELLS, KINASE OF, GAMMA; IKBKG *300249 : TRANSLOCASE OF INNER MITOCHONDRIAL MEMBRANE 17, YEAST, HOMOLOG OF, B; TIMM17B *300250 : ADRENAL UNRESPONSIVENESS TO ACTH ^300251 : MOVED TO 605875 *300252 : PEPTIDYL-PROLYL CIS/TRANS ISOMERASE, NIMA-INTERACTING, 4; PIN4 *300253 : SUPERCONSERVED RECEPTOR EXPRESSED IN BRAIN 3; SREB3 *300254 : SUPPRESSOR OF VARIEGATION 3-9, DROSOPHILA, HOMOLOG OF, 1; SUV39H1 *300255 : O-LINKED N-ACETYLGLUCOSAMINE TRANSFERASE; OGT *300256 : HYDROXYACYL-CoA DEHYDROGENASE, TYPE II; HADH2 #300257 : GLYCOGEN STORAGE DISEASE IIb 300258 : ROIFMAN SYNDROME 300259 : MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO INFECTION BY *300260 : LUBS X-LINKED MENTAL RETARDATION SYNDROME *300261 : ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME *300262 : ABIDI X-LINKED MENTAL RETARDATION SYNDROME *300263 : SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME *300264 : UBIQUILIN 2; UBQLN2 *300265 : ZINC FINGER PROTEIN OF CEREBELLUM, 3; ZIC3 *300266 : SPASTIC PARAPLEGIA 16, X-LINKED, COMPLICATED; SPG16 *300267 : RHO GUANINE NUCLEOTIDE EXCHANGE FACTOR 6; ARHGEF6 *300268 : ANGIONEUROTIC EDEMA, HEREDITARY, WITH NORMAL C1-INHIBITOR CONCENTRATION AND FUNCTION *300269 : HISTONE DEACETYLASE 8 300270 : ADRENOMYODYSTROPHY *300271 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 72; MRX72 *300272 : HISTONE DEACETYLASE 6; HDAC6 *300273 : GOITER, MULTINODULAR 2; MNG2 300274 : ANDROGEN INSENSITIVITY SYNDROME DUE TO COACTIVATOR DEFICIENCY *300275 : NAD(P)H STEROID DEHYDROGENASE-LIKE PROTEIN *300276 : ECTODYSPLASIN RECEPTOR, X-LINKED *300277 : INTERLEUKIN 1 RECEPTOR ACCESSORY PROTEIN-LIKE 2; IL1RAPL2 *300278 : NYCTALOPIN #300279 : MENTAL RETARDATION, X-LINKED, WITH PROGRESSIVE SPASTICITY 300280 : URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME *300281 : POTASSIUM VOLTAGE-GATED CHANNEL, SHAL-RELATED SUBFAMILY, MEMBER 1; KCND1 *300282 : CYTOSOLIC OVARIAN CARCINOMA ANTIGEN 1; COVA1 *300283 : INTERLEUKIN 1 RECEPTOR-ASSOCIATED KINASE 1; IRAK1 *300284 : RAS-ASSOCIATED PROTEIN RAB9; RAB9 *300285 : RAS-ASSOCIATED PROTEIN RAB9-LIKE *300286 : KRUPPEL-LIKE FACTOR 8; KLF8 *300287 : G ANTIGEN, FAMILY C, 1; GAGEC1 *300288 : G ANTIGEN, FAMILY B, 1; GAGEB1 *300289 : G ANTIGEN, FAMILY D, 2; GAGED2 300290 : INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, AND GENITAL ANOMALIES #300291 : ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH IMMUNE DEFICIENCY *300292 : FORKHEAD BOX P3 300293 : SPINA BIFIDA, X-LINKED *300294 : MEMBRANE-BOUND TRANSCRIPTION FACTOR PROTEASE, SITE 2; MBTPS2 *300295 : ONCOGENE PIM2; PIM2 *300296 : PLACENTA-SPECIFIC GENE 1; PLAC1 *300297 : APELIN *300298 : REGULATOR OF NONSENSE TRANSCRIPTS 3B #300299 : NEUTROPENIA, SEVERE CONGENITAL, X-LINKED; XLN *300300 : BRUTON AGAMMAGLOBULINEMIA TYROSINE KINASE; BTK #300301 : ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNODEFICIENCY, OSTEOPETROSIS, AND LYMPHEDEMA; OLEDAID *300302 : T COMPLEX-ASSOCIATED TESTIS-EXPRESSED 1-LIKE; TCTE1L *300303 : RIBOSOMAL PROTEIN S6 KINASE, 90-KD, 6; RPS6KA6 *300304 : CULLIN 4B; CUL4B *300305 : SPERM PROTEIN ASSOCIATED WITH THE NUCLEUS, X CHROMOSOME, FAMILY MEMBER A1; SPANXA1 *300306 : OBESITY QUANTITATIVE TRAIT LOCUS ON CHROMOSOME X *300307 : T-BOX 22; TBX22 *300308 : FERRITIN HEAVY POLYPEPTIDE-LIKE 17; FTHL17 *300309 : UBIQUITIN-SPECIFIC PROTEASE 26; USP26 *300310 : AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2; AGMX2 *300311 : TESTIS-EXPRESSED GENE 11; TEX11 *300312 : TESTIS-EXPRESSED GENE 13A; TEX13A *300313 : TESTIS-EXPRESSED GENE 13B; TEX13B *300314 : TAF7-LIKE RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 50-KD; TAF7L *300315 : NUCLEAR RNA EXPORT FACTOR 2; NXF2 *300316 : NUCLEAR RNA EXPORT FACTOR 3; NXF3 *300317 : RALBP1-ASSOCIATED EPS DOMAIN-CONTAINING PROTEIN 2; REPS2 *300318 : NUCLEAR RNA EXPORT FACTOR 4; NXF4 *300319 : NUCLEAR RNA EXPORT FACTOR 5; NXF5 *300320 : NTF2-RELATED EXPORT PROTEIN 2 *300321 : FG SYNDROME 2; FGS2 #300322 : LESCH-NYHAN SYNDROME; LNS #300323 : GOUT, HPRT-RELATED *300324 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 53; MRX53 *300325 : SYNOVIAL SARCOMA, X BREAKPOINT 3; SSX3 *300326 : SYNOVIAL SARCOMA, X BREAKPOINT 4; SSX4 *300327 : SYNOVIAL SARCOMA, X BREAKPOINT 5; SSX5 *300328 : POTASSIUM CHANNEL, VOLTAGE-GATED, ISK-RELATED FAMILY, MEMBER 1-LIKE; KCNE1L *300329 : KAISO GENE *300330 : SPERM PROTEIN ASSOCIATED WITH THE NUCLEUS, X CHROMOSOME, FAMILY MEMBER C; SPANXC *300331 : THROMBOCYTOSIS, FAMILIAL X-LINKED *300332 : INTEGRIN, BETA-1, BINDING PROTEIN OF, 2; ITGB1BP2 *300333 : RAS-ASSOCIATED PROTEIN RAB33A; RAB33A *300334 : TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY C, MEMBER 5; TRPC5 *300335 : ANGIOTENSIN I CONVERTING ENZYME 2; ACE2 *300336 : NEUROLIGIN 3; NLGN3 *300337 : HYPOMELANOSIS OF ITO; HMI *300338 : CYCLIC NUCLEOTIDE-GATED CHANNEL, ALPHA-2; CNGA2 *300339 : PROTEIN PHOSPHATASE 2A, REGULATORY SUBUNIT, 48-KD *300340 : MELANOMA ANTIGEN, FAMILY A, 5; MAGEA5 *300341 : MELANOMA ANTIGEN, FAMILY A, 8; MAGEA8 *300342 : MELANOMA ANTIGEN, FAMILY A, 9; MAGEA9 *300343 : MELANOMA ANTIGEN, FAMILY A, 10; MAGEA10 *300344 : MELANOMA ANTIGEN, FAMILY A, 11; MAGEA11 *300345 : MICROPHTHALMIA, COLOBOMATOUS *300346 : HIV-1 TAT STIMULATORY FACTOR 1; HTATSF1 *300347 : EARLY LYMPHOID ACTIVATION GENE *300348 : KELCH-LIKE 4; KLHL4 *300349 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, THETA; GABRQ *300350 : VENTROPTIN *300351 : GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED #300352 : CREATINE DEFICIENCY SYNDROME, X-LINKED *300353 : IMMUNOGLOBULIN SUPERFAMILY PROTEIN Z39IG *300354 : MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, SMALL TESTES, MUSCLE WASTING, AND TREMOR *300355 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, 73; MRX73 *300356 : TRANSLOCASE OF INNER MITOCHONDRIAL MEMBRANE 8, YEAST, HOMOLOG OF, A; TIMM8A *300357 : CYTOKINE RECEPTOR-LIKE FACTOR 2; CRLF2 *300358 : PROTEIN KINASE, LYSINE-DEFICIENT 3; PRKWNK3 *300359 : SARCOMA ANTIGEN *300360 : MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE *300361 : NERVE GROWTH FACTOR RECEPTOR-ASSOCIATED PROTEIN 1; NGFRAP1 *300362 : ARM PROTEIN LOST IN EPITHELIAL CANCERS, X CHROMOSOME, 1 *300363 : ARM PROTEIN LOST IN EPITHELIAL CANCERS, X CHROMOSOME, 2 *300364 : ARM PROTEIN LOST IN EPITHELIAL CANCERS, X CHROMOSOME, 3 *300365 : TOLL-LIKE RECEPTOR 7; TLR7 *300366 : TOLL-LIKE RECEPTOR 8; TLR8 #300367 : DYSERYTHROPOIETIC ANEMIA WITH THROMBOCYTOPENIA *300368 : SOLUTE CARRIER FAMILY 9, ISOFORM 7; SLC9A7 *300369 : ACIDIC REPEAT-CONTAINING GENE; ACRC *300370 : 3-PRIME @REPAIR EXONUCLEASE 2; TREX2 *300372 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, 42; MRX42 *300373 : OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS; OSCS *300374 : SH3-DOMAIN KINASE-BINDING PROTEIN 1; SH3KBP1 *300375 : CARBOHYDRATE SULFOTRANSFERASE 7; CHST7 #300376 : MUSCULAR DYSTROPHY, BECKER TYPE; BMD *300377 : DYSTROPHIN; DMD *300378 : RADIAL RAY DEFICIENCY, X-LINKED *300379 : PUTATIVE RING ZINC FINGER PROTEIN NY-REN-43 ANTIGEN *300380 : CYTIDINE 5-PRIME TRIPHOSPHATE SYNTHETASE 2; CTPS2 *300381 : ZINC FINGER PROTEIN 185; ZNF185 *300382 : ARISTALESS-RELATED HOMEOBOX, X-LINKED; ARX *300383 : PROPERDIN P FACTOR, COMPLEMENT; PFC *300384 : EMERIN; EMD *300385 : NUCLEOSOMAL BINDING PROTEIN 1; NSBP1 *300386 : TUMOR NECROSIS FACTOR LIGAND SUPERFAMILY, MEMBER 5; TNFSF5 #300387 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, 63; MRX63 *300388 : POLYMICROGYRIA, BILATERAL PERISYLVIAN #300389 : RETINITIS PIGMENTOSA 3; RP3 *300390 : CHOROIDEREMIA GENE; CHM *300391 : AMELOGENIN; AMELX *300392 : WAS GENE; WAS *300393 : G PROTEIN-COUPLED RECEPTOR 101; GPR101 *300394 : TAFAZZIN; TAZ *300395 : THO2, YEAST, HOMOLOG OF *300396 : CANCER/TESTIS ANTIGEN 2; CTAG2 #300397 : MENTAL RETARDATION, X-LINKED, WITH SEIZURES, SHORT STATURE, AND MIDFACE HYPOPLASIA *300398 : B-CELL RECEPTOR-ASSOCIATED PROTEIN, 31-KD *300399 : PROPROTEIN CONVERTASE, SUBTILISIN/KEXIN-TYPE, 1, INHIBITOR OF: PCSK1N #300400 : SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED; SCIDX1 *300500 : ALBINISM, OCULAR, TYPE I; OA1 *300600 : ALBINISM, OCULAR, TYPE II; OA2 300650 : ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS; OASD *300700 : ALBINISM-DEAFNESS SYNDROME; ADFN 300800 : ALBRIGHT HEREDITARY OSTEODYSTROPHY; AHO ^300900 : REMOVED FROM DATABASE #301000 : WISKOTT-ALDRICH SYNDROME; WAS #301040 : ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX #301050 : ALPORT SYNDROME, X-LINKED; ATS 301090 : AMELIA, X-LINKED *301100 : AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE; AIH #301200 : AMELOGENESIS IMPERFECTA 1, HYPOPLASTIC TYPE; AIH1 *301201 : AMELOGENESIS IMPERFECTA 3, HYPOPLASTIC TYPE; AIH3 *301220 : AMYLOIDOSIS, FAMILIAL CUTANEOUS *301300 : ANEMIA, SIDEROBLASTIC, X-LINKED #301310 : ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA; ASAT 301410 : ANENCEPHALY--SPINA BIFIDA *301500 : FABRY DISEASE *301590 : ANOPHTHALMOS, CLINICAL; ANOP1 301700 : ANOSMIA *301770 : ARRESTIN 3, RETINAL; ARR3 *301780 : ARYLSULFATASE C, ISOZYME F; ARSC2 301790 : ATAXIA-DEAFNESS SYNDROME, X-LINKED 301800 : ANUS, IMPERFORATE ^301810 : MOVED TO 215700 301815 : ARTHROGRYPOSIS, ECTODERMAL DYSPLASIA, CLEFT LIP/PALATE, AND DEVELOPMENTAL DELAY ^301820 : MOVED TO 208085 *301830 : ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED *301835 : ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION 301840 : ATAXIA-DEMENTIA SYNDROME *301845 : BAZEX SYNDROME; BZX 301850 : TUBULIN, BETA *301870 : BIGLYCAN; BGN ^301880 : REMOVED FROM DATABASE *301900 : BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS 301940 : BRACHYDACTYLY, MONONEN TYPE 301950 : BRANCHIAL ARCH SYNDROME, X-LINKED *302000 : BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE *302020 : CALBINDIN 3; CALB3 302030 : CALVARIAL HYPEROSTOSIS #302045 : CARDIOMYOPATHY, DILATED, X-LINKED; XLCM #302060 : BARTH SYNDROME; BTHS *302200 : CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES; CCT 302300 : CATARACT, CONGENITAL, WITH MICROCORNEA OR SLIGHT MICROPHTHALMIA *302350 : CATARACT-DENTAL SYNDROME 302380 : CATEL-MANZKE SYNDROME 302400 : CENTRAL INCISORS, ABSENCE OF *302500 : CEREBELLAR ATAXIA 2; CLA2 *302600 : CEREBELLAR ATAXIA WITH EXTRAPYRAMIDAL INVOLVEMENT *302650 : CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 1; CDR1 302700 : CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE #302800 : CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED; CMTX1 *302801 : CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED RECESSIVE, 2; CMTX2 *302802 : CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED RECESSIVE, 3; CMTX3 302803 : CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIA CUTIS CONGENITA 302900 : CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA, COMBINED 302905 : CHARGE-LIKE SYNDROME, X-LINKED *302910 : CHLORIDE CHANNEL 4; CLCN4 *302920 : CHOLESTEROL REPRESSIBLE PROTEIN 39C; CHR39C #302940 : CHONDRODYSPLASIA PUNCTATA, BRACHYTELEPHALANGIC #302950 : CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE; CDPX1 #302960 : CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2 #303100 : CHOROIDEREMIA; CHM 303110 : CHOROIDEREMIA WITH DEAFNESS AND OBESITY #303350 : MASA SYNDROME #303400 : CLEFT PALATE, X-LINKED; CPX #303600 : COFFIN-LOWRY SYNDROME; CLS *303630 : COLLAGEN, TYPE IV, ALPHA-5; COL4A5 *303631 : COLLAGEN, TYPE IV, ALPHA-6; COL4A6 303650 : COLONIC ATRESIA *303700 : COLORBLINDNESS, BLUE-MONO-CONE-MONOCHROMATIC TYPE; CBBM *303800 : COLORBLINDNESS, PARTIAL, DEUTAN SERIES; CBD *303900 : COLORBLINDNESS, PARTIAL, PROTAN SERIES; CBP 304000 : COLORBLINDNESS, PARTIAL TRITANOMALY #304020 : CONE DYSTROPHY, X-LINKED, 1; COD1 304030 : CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN *304040 : GAP JUNCTION PROTEIN, BETA-1; GJB1 *304050 : CORPUS CALLOSUM, AGENESIS OF, WITH CHORIORETINAL ABNORMALITY *304100 : CORPUS CALLOSUM, PARTIAL AGENESIS OF *304110 : CRANIOFRONTONASAL SYNDROME; CFNS #304120 : CRANIOORODIGITAL SYNDROME #304150 : CUTIS LAXA, X-LINKED 304200 : CUTIS VERTICIS GYRATA, THYROID APLASIA, AND MENTAL RETARDATION 304300 : CYANIDE, INABILITY TO SMELL *304340 : DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES 304350 : DEAFNESS-HYPOGONADISM SYNDROME; DHS #304400 : DEAFNESS, CONDUCTIVE, WITH STAPES FIXATION *304500 : DEAFNESS, X-LINKED 2, SENSORINEURAL CONGENITAL; DFN2 *304590 : DEAFNESS, HIGH-FREQUENCY SENSORINEURAL, X-LINKED ^304600 : MOVED TO 304590 #304700 : MOHR-TRANEBJAERG SYNDROME; MTS *304730 : DERMOIDS OF CORNEA; CND ^304750 : MOVED TO 306955 #304790 : IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX *304800 : DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED *304900 : DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE ^304930 : MOVED TO 304790 304950 : DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED ^304990 : REMOVED FROM DATABASE #305000 : DYSKERATOSIS CONGENITA, X-LINKED; DKC 305050 : DYSTONIA-DEAFNESS SYNDROME *305100 : ECTODERMAL DYSPLASIA 1, ANHIDROTIC; ED1 *305200 : EHLERS-DANLOS SYNDROME, TYPE V 305300 : ENDOCARDIAL FIBROELASTOSIS 305350 : EPIDERMODYSPLASIA VERRUCIFORMIS, X-LINKED; EDVX; EDV2 *305360 : MEMBRANE PROTEIN, PALMITOYLATED 1; MPP1 *305370 : TISSUE INHIBITOR OF METALLOPROTEINASE 1; TIMP1 *305371 : GATA-BINDING PROTEIN 1; GATA1 #305390 : EXUDATIVE VITREORETINOPATHY, FAMILIAL, X-LINKED RECESSIVE; EVR2 *305400 : FACIOGENITAL DYSPLASIA *305423 : FACTOR VIII-ASSOCIATED GENE 1 *305424 : FACTOR VIII-ASSOCIATED GENE 2 305425 : FARNESYL DIPHOSPHATE SYNTHASE-LIKE 5; FDPSL5 *305435 : F-CELL PRODUCTION 1; FCP1 *305450 : FG SYNDROME; FGS1 305550 : FINGERPRINT BODY MYOPATHY *305600 : FOCAL DERMAL HYPOPLASIA; DHOF *305620 : FRONTOMETAPHYSEAL DYSPLASIA 305645 : FRONTONASAL DYSPLASIA ^305650 : REMOVED FROM DATABASE *305660 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, ALPHA-3; GABRA3 *305670 : GASTRIN-RELEASING PEPTIDE RECEPTOR; GRPR 305690 : GENITOURINARY TRACT ANOMALIES 305700 : GERMINAL CELL APLASIA 305800 : GLOMERULONEPHRITIS, X-LINKED MESANGIOCAPILLARY *305900 : GLUCOSE-6-PHOSPHATE DEHYDROGENASE; G6PD ^305910 : MOVED TO 138130 *305915 : GLUTAMATE RECEPTOR, IONOTROPIC, AMPA 3; GRIA3 305920 : GLUTAMYL RIBOSE-5-PHOSPHATE STORAGE DISEASE ^305980 : MOVED TO 138140 *305990 : GLYCINE RECEPTOR, ALPHA-2 SUBUNIT; GLRA2 *306000 : GLYCOGEN STORAGE DISEASE VIII *306100 : GONADAL DYSGENESIS, XY FEMALE TYPE; GDXY #306190 : GONADOTROPIN DEFICIENCY; GTD *306250 : COLONY-STIMULATING FACTOR 2 RECEPTOR, ALPHA; CSF2RA 306300 : GRANULOMAS, CONGENITAL CEREBRAL *306400 : GRANULOMATOUS DISEASE, CHRONIC; CGD *306480 : DXF68S1E 306500 : GYNECOMASTIA, FAMILIAL ^306600 : REMOVED FROM DATABASE *306700 : HEMOPHILIA A 306800 : HEMOPHILIA A WITH VASCULAR ABNORMALITY *306900 : HEMOPHILIA B; HEMB 306930 : HEMOPOIETIC PROLIFERATION 306950 : HERNIA, ANTERIOR DIAPHRAGMATIC #306955 : HETEROTAXY, VISCERAL, X-LINKED 306960 : HHHH SYNDROME 306970 : H-Y REGULATOR; HYR 306980 : HIRSCHSPRUNG DISEASE WITH TYPE D BRACHYDACTYLY 306990 : HOLOPROSENCEPHALY WITH FETAL AKINESIA/HYPOKINESIA SEQUENCE 306995 : HOMOSEXUALITY 1; HMS1 #307000 : HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS; HSAS1; HSAS; HYCX 307010 : HYDROCEPHALUS WITH CEREBELLAR AGENESIS *307030 : HYPERGLYCEROLEMIA *307150 : HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2 #307200 : HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED 307300 : HYPOGONADISM, MALE 307500 : HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES ^307600 : MOVED TO 602014 *307700 : HYPOPARATHYROIDISM, X-LINKED; HYPX *307800 : HYPOPHOSPHATEMIA, X-LINKED #307810 : HYPOPHOSPHATEMIA, HEREDITARY, TYPE II 307830 : HYPOURICEMIA, FAMILIAL RENAL, DUE TO TUBULAR HYPERSECRETION *308000 : HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1 #308050 : CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS *308100 : ICHTHYOSIS, X-LINKED 308200 : ICHTHYOSIS AND MALE HYPOGONADISM *308205 : ICHTHYOSIS FOLLICULARIS, ATRICHIA, AND PHOTOPHOBIA SYNDROME ^308210 : REMOVED FROM DATABASE 308220 : IMMUNODEFICIENCY, X-LINKED, WITH DEFICIENCY OF 115,000 DALTON SURFACE GLYCOPROTEIN #308230 : IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 1; HIGM1 *308240 : LYMPHOPROLIFERATIVE SYNDROME *308250 : IMMUNOGLOBULIN M, LEVEL OF 308280 : IMPACTED TEETH, MULTIPLE 308290 : IMPRINTING GENE RELATED TO RETINOBLASTOMA #308300 : INCONTINENTIA PIGMENTI; IP ^308310 : MOVED TO 308300 #308350 : INFANTILE SPASM SYNDROME, X-LINKED #308370 : INFERTILE MALE SYNDROME *308380 : INTERLEUKIN 2 RECEPTOR, GAMMA; IL2RG *308385 : INTERLEUKIN 3 RECEPTOR, ALPHA; IL3RA 308400 : REMOVED FROM DATABASE 308500 : IRIS, HYPOPLASIA OF, WITH GLAUCOMA; IHG 308600 : JAUNDICE, FAMILIAL OBSTRUCTIVE, OF INFANCY *308700 : KALLMANN SYNDROME 1; KAL1 308750 : KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA *308800 : KERATOSIS FOLLICULARIS SPINULOSA DECALVANS CUM OPHIASI; KFSD 308830 : KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY *308840 : L1 CELL ADHESION MOLECULE; L1CAM 308850 : LARYNGEAL ABDUCTOR PARALYSIS 308905 : LEBER OPTIC ATROPHY, SUSCEPTIBILITY TO 308930 : LEIGH SYNDROME, X-LINKED #308940 : LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY 308950 : LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT 308960 : LEUKEMIA, ACUTE, ?X-LINKED ^308980 : MOVED TO 151660 308990 : LOW MOLECULAR WEIGHT PROTEINURIA, ASYMPTOMATIC; LMWP *309000 : LOWE OCULOCEREBRORENAL SYNDROME; OCRL *309050 : LUTHERAN SUPPRESSOR, X-LINKED; XS *309060 : LYSOSOME-ASSOCIATED MEMBRANE PROTEIN 2; LAMP2 *309100 : MACULAR DYSTROPHY, X-LINKED 309120 : MALE INFERTILITY FROM DEFECT IN MEIOSIS *309150 : MALE PSEUDOHERMAPHRODITISM: DEFICIENCY OF TESTICULAR 17,20-DESMOLASE; TDD *309200 : MAJOR AFFECTIVE DISORDER 2; MAFD2 *309300 : MEGALOCORNEA; MGC1 309350 : MELNICK-NEEDLES OSTEODYSPLASTY #309400 : MENKES SYNDROME #309470 : SUTHERLAND-HAAN X-LINKED MENTAL RETARDATION SYNDROME; SHS 309480 : MENTAL RETARDATION ASSOCIATED WITH PSORIASIS 309490 : MENTAL RETARDATION WITH DISTINCTIVE MOUTH, OBESITY, AND HYPOGONADISM *309500 : RENPENNING SYNDROME 1; RENS1 #309510 : PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS *309520 : MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS #309530 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 1; MRX1 ^309540 : MOVED TO 309548 #309541 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 3; MRX3 *309545 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, WITH APHASIA; MRXA *309548 : FRAGILE SITE, FOLIC ACID TYPE, RARE, FRA(X)(q28); FRAXE 309549 : MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 9; MRX9 *309550 : FRAGILE SITE MENTAL RETARDATION 1; FMR1 *309555 : MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES 309560 : MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS #309580 : MENTAL RETARDATION, SMITH-FINEMAN-MYERS TYPE *309583 : MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE *309585 : WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS #309590 : MENTAL RETARDATION, X-LINKED, WITH GROWTH RETARDATION, DEAFNESS, AND MICROGENITALISM *309600 : MENTAL RETARDATION, X-LINKED, WITH HYPOTONIA *309605 : MILES-CARPENTER X-LINKED MENTAL RETARDATION SYNDROME; MCS *309610 : PRIETO X-LINKED MENTAL RETARDATION SYNDROME; PRS *309620 : MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD *309630 : METACARPAL 4-5 FUSION; MF4 309640 : MENTAL RETARDATION WITH SPASTIC PARAPLEGIA 309645 : METAPHYSEAL ANADYSPLASIA 309660 : MENTAL RETARDATION, SCAPULOPERONEAL MUSCULAR DYSTROPHY, AND LETHAL CARDIOMYOPATHY 309700 : MICROPHTHALMIA *309800 : MICROPHTHALMIA WITH ASSOCIATED ANOMALIES; MAA *309801 : MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS 309840 : MODIFIER, X-LINKED, FOR NEUROFUNCTIONAL DEFECTS *309845 : MOESIN; MSN *309850 : MONOAMINE OXIDASE A; MAOA *309860 : MONOAMINE OXIDASE B; MAOB *309900 : MUCOPOLYSACCHARIDOSIS TYPE II 309930 : MUSCULAR DYSTROPHY, CARDIAC TYPE 309950 : MUSCULAR DYSTROPHY, HEMIZYGOUS LETHAL TYPE 310000 : MUSCULAR DYSTROPHY, MABRY TYPE 310095 : MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL #310200 : MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD #310300 : EMERY-DREIFUSS MUSCULAR DYSTROPHY; EDMD ^310305 : MOVED TO 601415 *310310 : MYCL-RELATED PROCESSED GENE; MYCL2 310350 : MYELOLYMPHATIC INSUFFICIENCY 310370 : MYOCLONIC EPILEPSY, PROGRESSIVE *310400 : MYOTUBULAR MYOPATHY 1; MTM1 *310440 : MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX 310450 : MYOPATHY, QUADRICEPS *310460 : MYOPIA 1; MYP1 310465 : N SYNDROME; NSX #310468 : NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE; XRN 310470 : NEUROPATHY, HEREDITARY SENSORY, X-LINKED *310490 : NEUROPATHY, AXONAL MOTOR-SENSORY, WITH DEAFNESS AND MENTAL RETARDATION; NAMSD #310500 : NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1; CSNB1 *310600 : NORRIE DISEASE; NDP 310650 : NUCLEAR RIBONUCLEIC ACID; nRNA *310700 : NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1 310800 : NYSTAGMUS, MYOCLONIC 310900 : OCCIPITAL HAIR, WHITE LOCK OF 310980 : OMPHALOCELE ^310990 : MOVED TO 190020 *311000 : OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA; OPEM *311010 : V-RAF MURINE SARCOMA 3611 VIRAL ONCOGENE HOMOLOG 1; ARAF1 ^311020 : MOVED TO 311010 *311030 : MCF.2 CELL LINE DERIVED TRANSFORMING SEQUENCE; MCF2 *311040 : ELK1, MEMBER OF ETS ONCOGENE FAMILY; ELK1 *311050 : OPTIC ATROPHY 2; OPA2 311070 : OPTIC ATROPHY, POLYNEUROPATHY, AND DEAFNESS 311100 : OPTIC ATROPHY--SPASTIC PARAPLEGIA SYNDROME #311150 : OPTICOACOUSTIC NERVE ATROPHY WITH DEMENTIA #311200 : OROFACIODIGITAL SYNDROME I; OFD1 *311240 : ORNITHINE AMINOTRANSFERASE-LIKE 1; OATL1 *311241 : ORNITHINE AMINOTRANSFERASE-LIKE 2; OATL2 *311250 : ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO; OTC 311280 : OSTEOPATHIA STRIATA WITH PIGMENTARY DERMOPATHY INCLUDING WHITE FORELOCK *311300 : OTOPALATODIGITAL SYNDROME 311350 : OUABAIN RESISTANCE; OUBR #311360 : PREMATURE OVARIAN FAILURE, X-LINKED 311400 : PAINE SYNDROME 311450 : PALLISTER W SYNDROME *311510 : PARKINSONISM, EARLY-ONSET, WITH MENTAL RETARDATION *311550 : PCTAIRE PROTEIN KINASE 1; PCTK1 311601 : PELIZAEUS-MERZBACHER-LIKE DISEASE; PMLD ^311700 : REMOVED FROM DATABASE 311750 : PERIODONTOSIS *311770 : PHOSPHATIDYLINOSITOL GLYCAN, CLASS A; PIGA *311790 : 6-@PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE 1; PFKFB1 *311800 : PHOSPHOGLYCERATE KINASE 1; PGK1 ^311810 : MOVED TO 311800 *311850 : PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE I; PRPS1 *311860 : PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE II; PRPS2 *311870 : PHOSPHORYLASE KINASE, MUSCLE, ALPHA-1 SUBUNIT; PHKA1 311895 : PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES 311900 : PIERRE ROBIN SYNDROME WITH CONGENITAL HEART MALFORMATION AND CLUBFOOT *312000 : PANHYPOPITUITARISM; PHP 312030 : PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN, X-LINKED; B1G2; SP1X *312040 : POLYMERASE, DNA, ALPHA; POLA #312060 : PROPERDIN DEFICIENCY, X-LINKED *312070 : UBIQUITIN-LIKE 4; UBL4 *312080 : PROTEOLIPID PROTEIN 1; PLP1 *312090 : PROTEIN P3 *312095 : PSEUDOAUTOSOMAL GENE XE7 312100 : PSEUDOHERMAPHRODITISM, INCOMPLETE MALE, TYPE I 312150 : PTERYGIUM SYNDROME, MULTIPLE, X-LINKED *312170 : PYRUVATE DEHYDROGENASE COMPLEX, E1-ALPHA POLYPEPTIDE 1; PDHA1 *312173 : RIBOSOMAL PROTEIN L10; RPL10 *312180 : UBIQUITIN-CONJUGATING ENZYME E2A; UBE2A 312190 : RADIAL APLASIA, X-LINKED 312200 : RADIAL LOOP, PLAIN, ON RIGHT INDEX FINGER 312210 : RADIATION SENSITIVITY OF NATURAL KILLER ACTIVITY #312300 : REIFENSTEIN SYNDROME ^312390 : MOVED TO 314310 ^312400 : MOVED TO 604278 *312420 : RENIN-BINDING PROTEIN; RENBP 312450 : RESPIRATION DEFICIENCY *312500 : RETICULOENDOTHELIOSIS, X-LINKED 312530 : RETINAL DETACHMENT 312550 : RETINAL DYSPLASIA, PRIMARY; PRD *312600 : RETINITIS PIGMENTOSA 2; RP2 *312610 : RETINITIS PIGMENTOSA GTPase REGULATOR; RPGR 312612 : RETINITIS PIGMENTOSA 6; RP6 *312700 : RETINOSCHISIS 1, X-LINKED, JUVENILE; RS1 #312750 : RETT SYNDROME; RTT *312760 : RIBOSOMAL PROTEIN S4, X-LINKED; RPS4X 312780 : RUSSELL-SILVER SYNDROME, X-LINKED 312800 : SACRAL DEFECT WITH ANTERIOR SACRAL MENINGOCELE *312820 : SARCOMA, SYNOVIAL, X BREAKPOINT 1; SSX1 312830 : SCARF SYNDROME 312840 : SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME 312860 : SCOTT CRANIODIGITAL SYNDROME WITH MENTAL RETARDATION *312861 : 5-@HYDROXYTRYPTAMINE RECEPTOR 2C; HTR2C #312863 : COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX *312865 : SHORT STATURE HOMEO BOX; SHOX #312870 : SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1 312890 : SPASTIC ATHETOTIC PARAPLEGIA #312900 : SPASTIC PARAPLEGIA 1, X-LINKED, COMPLICATED; SPG1 312910 : SPASTIC PARAPARESIS AND DEAFNESS #312920 : SPASTIC PARAPLEGIA 2, X-LINKED, UNCOMPLICATED; SPG2 *313000 : SPATIAL VISUALIZATION, APTITUDE FOR *313020 : SPERMIDINE/SPERMINE N(1)-ACETYLTRANSFERASE; SAT ^313100 : MOVED TO 605041 #313200 : SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1; SMAX1 *313350 : SPLIT-HAND/FOOT MALFORMATION 2; SHFM2 #313400 : SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED *313420 : SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED *313430 : SRY-BOX 3; SOX3 *313440 : SYNAPSIN I; SYN1 *313450 : SURFACE ANTIGEN, X-LINKED; SAX 313460 : SURFACE ANTIGEN, X-LINKED, SECOND; SAX2 *313470 : SURFACE ANTIGEN MIC2; MIC2 *313475 : SYNAPTOPHYSIN; SYP *313480 : TaqI POLYMORPHISM; TAQ1 313490 : TAURODONTISM, MICRODONTIA, AND DENS INVAGINATUS 313500 : OLIGODONTIA 1; ODT1 313550 : TEETH, BURIED *313650 : TAF1 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 250-KD; TAF1 ^313680 : MOVED TO 187395 *313700 : ANDROGEN RECEPTOR; AR *313850 : THORACOABDOMINAL SYNDROME; THAS #313900 : THROMBOCYTOPENIA 1; THC1 314000 : THROMBOCYTOPENIA WITH ELEVATED SERUM IgA AND RENAL DISEASE *314050 : THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCED GLOBIN SYNTHESIS 314100 : THUMBS, CONGENITAL CLASPED *314200 : THYROXINE-BINDING GLOBULIN OF SERUM; TBG 314240 : TOOTH SIZE *314250 : DYSTONIA 3, TORSION, X-LINKED; DYT3 *314300 : TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR *314310 : TRANSCRIPTION FACTOR FOR IMMUNOGLOBULIN HEAVY-CHAIN ENHANCER 3; TFE3 314320 : TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY 314350 : TYROSINE AMINOTRANSFERASE, REGULATOR OF 314360 : ULNAR HYPOPLASIA WITH LOBSTER-CLAW DEFORMITY OF FEET *314370 : UBIQUITIN-ACTIVATING ENZYME 1; UBE1 *314375 : SOLUTE CARRIER FAMILY 35, MEMBER 2; SLC35A2 *314380 : UNIQUE GREEN PHENOMENON *314390 : VACTERL ASSOCIATION WITH HYDROCEPHALUS, X-LINKED *314400 : CARDIAC VALVULAR DYSPLASIA, X-LINKED *314500 : VAN DEN BOSCH SYNDROME 314550 : VESICOURETERAL REFLUX; VUR ^314555 : MOVED TO 604492 314560 : VON WILLEBRAND DISEASE, X-LINKED FORM 314570 : WIDOW'S PEAK SYNDROME *314580 : WIEACKER SYNDROME 314600 : WILDERVANCK SYNDROME *314670 : X INACTIVATION-SPECIFIC TRANSCRIPT; XIST *314690 : SELECTED cDNA ON X, MOUSE, HOMOLOG OF; SMCX *314700 : XG BLOOD GROUP SYSTEM; XG; PBDX *314705 : XG REGULATOR; XGR 314800 : XH ANTIGEN *314850 : KELL BLOOD GROUP PRECURSOR; XK *314900 : XM SYSTEM 314920 : XP24 314940 : XP37 314960 : XP40 *314980 : ZINC FINGER PROTEIN, X-LINKED; ZFX *314990 : ZINC FINGER PROTEIN 6; ZNF6 *314993 : ZINC FINGER PROTEIN 21; ZNF21 *314995 : ZINC FINGER PROTEIN 41; ZNF41 *314997 : ZINC FINGER PROTEIN 75; ZNF75 *314998 : ZINC FINGER PROTEIN 81; ZNF81 315000 : ZONULAR CATARACT AND NYSTAGMUS *400000 : AZOOSPERMIA FACTOR 2; AZF2 ^400001 : MOVED TO 426000 ^400002 : MOVED TO 314700 *400003 : DELETED IN AZOOSPERMIA; DAZ *400004 : RETINITIS PIGMENTOSA, Y-LINKED *400005 : UBIQUITIN-SPECIFIC PROTEASE 9, Y CHROMOSOME; USP9Y *400006 : RNA-BINDING MOTIF PROTEIN, Y CHROMOSOME, FAMILY 1, MEMBER A1; RBMY1A1 ^400007 : MOVED TO 400006 *400008 : PROTEIN KINASE, Y-LINKED; PRKY *400009 : UBIQUITOUSLY TRANSCRIBED TETRATRICOPEPTIDE REPEAT GENE ON Y CHROMOSOME; UTY *400010 : DEAD/H BOX 3, Y-LINKED; DBY *400011 : ACETYLSEROTONIN METHYLTRANSFERASE-LIKE, Y-LINKED *400012 : VARIABLY CHARGED, Y CHROMOSOME; VCY *400013 : BASIC PROTEIN ON Y CHROMOSOME, 2 *400014 : EUKARYOTIC TRANSLATION INITIATION FACTOR 1A, Y ISOFORM; EIF1AY *400015 : XK-RELATED PROTEIN ON Y CHROMOSOME *400016 : CHROMODOMAIN PROTEIN, Y CHROMOSOME, 1; CDY1 *400017 : THYMOSIN, BETA-4, Y CHROMOSOME; TMSB4Y *400018 : CHROMODOMAIN PROTEIN, Y CHROMOSOME, 2; CDY2 *400019 : PTPBL-RELATED PROTEIN ON Y; PRY *400020 : SHORT STATURE HOMEO BOX, Y-LINKED; SHOXY *400021 : HODGKIN DISEASE, Y-LINKED PSEUDOAUTOSOMAL *400022 : PROTOCADHERIN 11, Y-LINKED; PCDH11Y *400023 : CYTOKINE RECEPTOR-LIKE FACTOR 2, Y-LINKED; CRLF2Y *400024 : AZOOSPERMIA FACTOR C *402500 : ACETYLSEROTONIN METHYLTRANSFERASE, Y-CHROMOSOMAL; ASMT *403000 : ADENINE NUCLEOTIDE TRANSLOCATOR 3, Y-CHROMOSOMAL; ANT3Y *410000 : AMELOGENIN, Y-CHROMOSOMAL; AMELY *415000 : AZOOSPERMIA FACTOR 1; AZF1 ^424000 : REMOVED FROM DATABASE *424500 : GONADOBLASTOMA; GBY *425000 : GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR RECEPTOR, ALPHA SUBUNIT, Y-CHROMOSOMAL; CSF2RY 425500 : HAIRY EARS, Y-LINKED *426000 : SELECTED cDNA ON Y, MOUSE, HOMOLOG OF; SMCY *430000 : INTERLEUKIN 3 RECEPTOR, Y-CHROMOSOMAL; IL3RA *450000 : MIC2 SURFACE ANTIGEN, Y-CHROMOSOMAL; MIC2Y *465000 : PSEUDOAUTOSOMAL GENE XE7, Y-CHROMOSOMAL; XE7Y *470000 : RIBOSOMAL PROTEIN S4, Y-LINKED; RPS4Y *475000 : GROWTH CONTROL, Y-CHROMOSOME INFLUENCED; GCY *480000 : SEX-DETERMINING REGION Y; SRY *480100 : TESTIS-SPECIFIC PROTEIN, Y-ENCODED; TSPY ^488000 : MOVED TO 475000 489000 : UBIQUITIN-ACTIVATING ENZYME, Y-LINKED *489500 : XG REGULATOR; XGR *490000 : ZINC FINGER PROTEIN, Y-LINKED; ZFY #500000 : CARDIOMYOPATHY, INFANTILE HISTIOCYTOID #502000 : AGING #502500 : ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL #510000 : CARDIOMYOPATHY, IDIOPATHIC DILATED, MITOCHONDRIAL #515000 : CHLORAMPHENICOL TOXICITY *516000 : COMPLEX I, SUBUNIT ND1; MTND1 *516001 : COMPLEX I, SUBUNIT ND2; MTND2 *516002 : COMPLEX I, SUBUNIT ND3; MTND3 *516003 : COMPLEX I, SUBUNIT ND4; MTND4 *516004 : COMPLEX I, SUBUNIT ND4L; MTND4L *516005 : COMPLEX I, SUBUNIT ND5; MTND5 *516006 : COMPLEX I, SUBUNIT ND6; MTND6 *516020 : CYTOCHROME b OF COMPLEX III; MTCYB *516030 : COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT I; MTCO1 *516040 : COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT II; MTCO2 *516050 : CYTOCHROME c OXIDASE III; MTCO3 *516060 : ATP SYNTHASE 6; MTATP6 *516070 : ATP SYNTHASE 8; MTATP8 #520000 : DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED #520100 : DIARRHEA, CHRONIC, WITH VILLOUS ATROPHY #530000 : KEARNS-SAYRE SYNDROME; KSS #535000 : LEBER OPTIC ATROPHY #540000 : MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKELIKE EPISODES; MELAS #545000 : MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS; MERRF #550000 : MITOCHONDRIAL DNA BREAKAGE SYNDROME, SECONDARY TO NUCLEAR MUTATION #550500 : MYOGLOBINURIA, RECURRENT ^550900 : MOVED TO 603041 #551000 : MYOPATHY, MITOCHONDRIAL, LETHAL INFANTILE; LIMM #551200 : NEPHROPATHY, CHRONIC TUBULOINTERSTITIAL #551500 : NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA #553000 : ONCOCYTOMA #555000 : OPHTHALMOPLEGIA, PROGRESSIVE EXTERNAL, AND SCOLIOSIS #556500 : PARKINSON DISEASE #557000 : PEARSON MARROW-PANCREAS SYNDROME #560000 : RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA DUE TO DUPLICATION OF MITOCHONDRIAL DNA *561000 : RIBOSOMAL RNA, MITOCHONDRIAL, 12S; MTRNR1 *561010 : RIBOSOMAL RNA, MITOCHONDRIAL, 16S; MTRNR2 #580000 : STREPTOMYCIN OTOTOXICITY *590000 : TRANSFER RNA, MITOCHONDRIAL, ALANINE; MTTA *590005 : TRANSFER RNA, MITOCHONDRIAL, ARGININE; MTTR *590010 : TRANSFER RNA, MITOCHONDRIAL, ASPARAGINE; MTTN *590015 : TRANSFER RNA, MITOCHONDRIAL, ASPARTIC ACID; MTTD *590020 : TRANSFER RNA, MITOCHONDRIAL, CYSTEINE; MTTC *590025 : TRANSFER RNA, MITOCHONDRIAL, GLUTAMIC ACID; MTTE *590030 : TRANSFER RNA, MITOCHONDRIAL, GLUTAMINE; MTTQ *590035 : TRANSFER RNA, MITOCHONDRIAL, GLYCINE; MTTG *590040 : TRANSFER RNA, MITOCHONDRIAL, HISTIDINE; MTTH *590045 : TRANSFER RNA, MITOCHONDRIAL, ISOLEUCINE; MTTI *590050 : TRANSFER RNA, MITOCHONDRIAL, LEUCINE, 1; MTTL1 *590055 : TRANSFER RNA, MITOCHONDRIAL, LEUCINE, 2; MTTL2 *590060 : TRANSFER RNA, MITOCHONDRIAL, LYSINE; MTTK *590065 : TRANSFER RNA, MITOCHONDRIAL, METHIONINE; MTTM *590070 : TRANSFER RNA, MITOCHONDRIAL, PHENYLALANINE; MTTF *590075 : TRANSFER RNA, MITOCHONDRIAL, PROLINE; MTTP *590080 : TRANSFER RNA, MITOCHONDRIAL, SERINE, 1; MTTS1 *590085 : TRANSFER RNA, MITOCHONDRIAL, SERINE, 2; MTTS2 *590090 : TRANSFER RNA, MITOCHONDRIAL, THREONINE; MTTT *590095 : TRANSFER RNA, MITOCHONDRIAL, TRYPTOPHAN; MTTW *590100 : TRANSFER RNA, MITOCHONDRIAL, TYROSINE; MTTY *590105 : TRANSFER RNA, MITOCHONDRIAL, VALINE; MTTV #598500 : WOLFRAM SYNDROME, MITOCHONDRIAL FORM 600000 : SPONDYLOCAMPTODACTYLY 600001 : PANCREATIC HYPOPLASIA, CONGENITAL, WITH DIABETES MELLITUS AND CONGENITAL HEART DISEASE 600002 : EIKEN SKELETAL DYSPLASIA *600003 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, BETA-2 SUBUNIT; CACNB2 *600004 : EPHRIN RECEPTOR EphA5; EPHA5 *600005 : MAJOR HISTOCOMPATIBILITY COMPLEX CLASS II TRANSACTIVATOR; MHC2TA *600006 : REGULATORY FACTOR X, 1; RFX1 *600007 : FMS-RELATED TYROSINE KINASE 3 LIGAND; FLT3LG *600008 : NICOTINAMIDE N-METHYLTRANSFERASE; NNMT *600009 : INTERFERON-ALPHA-INDUCIBLE PROTEIN 27; IFI27 *600010 : INSULINOMA-ASSOCIATED 1; INSM1 *600011 : EPHRIN RECEPTOR EphB4; EPHB4 *600012 : UBIQUITIN-CONJUGATING ENZYME E2L 1; UBE2L1 *600013 : TRANSCRIPTION FACTOR YY1; YY1 *600014 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY A, MEMBER 2; SMARCA2 ^600015 : MOVED TO 106165 *600016 : CONTACTIN 1; CNTN1 *600017 : SYNDECAN 4; SDC4 *600018 : OPIOID RECEPTOR, MU-1; OPRM1 *600019 : CYTOCHROME b561; CYB561 *600020 : MAX-INTERACTING PROTEIN 1; MXI1 *600021 : MAX DIMERIZATION PROTEIN; MAD *600022 : PROSTAGLANDIN I2 RECEPTOR; PTGIR *600023 : CADHERIN 11; CDH11 *600024 : LAMIN B RECEPTOR; LBR *600025 : KINESIN 2; KNS2 *600026 : SYNTROPHIN, BETA-1; SNTB1 *600027 : SYNTROPHIN, BETA-2; SNTB2 *600028 : DISTAL-LESS HOMEO BOX 5; DLX5 *600029 : DISTAL-LESS HOMEO BOX 1; DLX1 *600030 : DISTAL-LESS HOMEO BOX 6; DLX6 *600031 : CHITINASE 1; CHIT1 ^600032 : MOVED TO 182455 *600033 : TISSUE FACTOR PATHWAY INHIBITOR 2 *600034 : EMPTY SPIRACLES, DROSOPHILA, HOMOLOG OF, 1; EMX1 *600035 : EMPTY SPIRACLES, DROSOPHILA, 2, HOMOLOG OF; EMX2 *600036 : ORTHODENTICLE, DROSOPHILA, HOMOLOG 1; OTX1 *600037 : ORTHODENTICLE, DROSOPHILA, HOMOLOG OF, 2; OTX2 *600038 : MEGAKARYOCTYE-ASSOCIATED TYROSINE KINASE; MATK *600039 : BCL2-LIKE 1; BCL2L1 *600040 : BCL2-ASSOCIATED X PROTEIN; BAX *600041 : PURINERGIC RECEPTOR P2Y, G PROTEIN-COUPLED, 2; P2RY2 *600042 : MELANOCORTIN 5 RECEPTOR; MC5R *600043 : SULFOTRANSFERASE, ESTROGEN-PREFERRING; STE *600044 : THROMBOPOIETIN; THPO *600045 : DNA DAMAGE-BINDING PROTEIN 1; DDB1 *600046 : ATP-BINDING CASSETTE, SUBFAMILY A, MEMBER 1; ABCA1 *600047 : ATP-BINDING CASSETTE, SUBFAMILY A, MEMBER 2; ABCA2 *600048 : BREAST CANCER, 11-22 TRANSLOCATION ASSOCIATED *600049 : MYELODYSPLASIA SYNDROME 1; MDS1 *600050 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 11; MAP3K11 *600051 : EPIDERMAL GROWTH FACTOR RECEPTOR PATHWAY SUBSTRATE-15; EPS15 *600052 : ANGIOTENSIN RECEPTOR-LIKE 1; AGTRL1 *600053 : CYCLIC NUCLEOTIDE-GATED CHANNEL, ALPHA-3; CNGA3 ^600054 : MOVED TO 300338 ^600055 : MOVED TO 426000 ^600056 : MOVED TO 314690 600057 : EXSTROPHY OF BLADDER *600058 : PROTEIN TYROSINE KINASE TXK; TXK *600059 : RETINITIS PIGMENTOSA 13; RP13 #600060 : DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 2; DFNB2 *600061 : RAD23, YEAST, HOMOLOG OF, A; RAD23A *600062 : RAD23, YEAST, HOMOLOG OF, B; RAD23B *600063 : AUTOANTIGEN Ro/SSA, 60-KD; RO60 *600064 : HAIR FOLLICLE SPECIFIC GENE 1; HACL1 *600065 : INTEGRIN, BETA-2; ITGB2 *600066 : EPHRIN RECEPTOR EphA6; EPHA6 *600067 : URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASE 2 FAMILY, MEMBER B4; UGT2B4 *600068 : URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASE 2 FAMILY, MEMBER B7; UGT2B7 *600069 : URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASE 2 FAMILY, MEMBER B15; UGT2B15 *600070 : URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASE 2 FAMILY, MEMBER B10; UGT2B10 ^600071 : MOVED TO 600067 #600072 : FAMILIAL FATAL INSOMNIA; FFI *600073 : LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 2; LRP2 *600074 : CD24 ANTIGEN; CD24 *600075 : TATA BOX-BINDING PROTEIN; TBP *600076 : TENSIN; TNS ^600077 : MOVED TO 224750 ^600078 : MOVED TO 300012 *600079 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 12; PTPN12 600080 : MYELOCYTIC LEUKEMIA-LIKE SYNDROME, FAMILIAL, CHRONIC 600081 : VITAMIN D 25-HYDROXYLATION, RICKETS DUE TO DEFECT IN 600082 : PROSTATIC HYPERPLASIA, BENIGN; BPH ^600083 : MOVED TO 300144 600084 : MACROCYTOSIS, FAMILIAL *600085 : PROTEIN-TYROSINE KINASE SYK; SYK *600086 : ALCOHOL DEHYDROGENASE 7; ADH7 *600087 : TUFTELIN; TUFT1 #600088 : DYSTONIA MUSCULORUM OF MOUSE, HUMAN HOMOLOG OF; DMH; D6S1101 600089 : PANCREATIC BETA CELL AGENESIS WITH NEONATAL DIABETES MELLITUS ^600090 : MOVED TO 300013 600091 : SPINAL MUSCULAR ATROPHY, PROXIMAL, CHILDHOOD-ONSET, AUTOSOMAL DOMINANT 600092 : CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME 600093 : SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES ^600094 : MOVED TO 300095 *600095 : SPLIT-HAND/FOOT MALFORMATION 3; SHFM3 600096 : PUERTO RICAN INFANT HYPOTONIA SYNDROME ^600097 : MOVED TO 300106 *600098 : RELATED RAS VIRAL ONCOGENE HOMOLOG 2; RRAS2 ^600099 : MOVED TO 246530 ^600100 : MOVED TO 601792 #600101 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 2; DFNA2 ^600102 : MOVED TO 300067 *600103 : SYNAPTOTAGMIN 4; SYT4 *600104 : SYNAPTOTAGMIN 2; SYT2 #600105 : RETINITIS PIGMENTOSA 12; RP12 *600106 : INOSITOL POLYPHOSPHATE-5-PHOSPHATASE, 40-KD; INPP5A ^600107 : MOVED TO 300014 *600108 : MATRIX METALLOPROTEINASE 13; MMP13 *600109 : PROXIMAL MYOTONIC MYOPATHY; PROMM #600110 : STARGARDT DISEASE 3; STGD3 *600111 : SOLUTE CARRIER FAMILY 1 (GLIAL HIGH AFFINITY GLUTAMATE TRANSPORTER), MEMBER 3; SLC1A3 *600112 : DYNEIN, CYTOPLASMIC, HEAVY CHAIN 1; DNCH1 ^600113 : MOVED TO 300005 *600114 : CHAPERONIN CONTAINING T-COMPLEX POLYPEPTIDE 1, SUBUNIT 3; CCT3 ^600115 : MOVED TO 163260 #600116 : PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ 600117 : DYSPHASIA, FAMILIAL DEVELOPMENTAL 600118 : WARBURG MICRO SYNDROME *600119 : SARCOGLYCAN, ALPHA; SGCA ^600120 : MOVED TO 186100 #600121 : RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 3; RCDP3 600122 : MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE 600123 : ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL AND RADIAL DEFECTS *600124 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN A2/B1; HNRPA2B1 ^600125 : MOVED TO 126065 *600126 : PHOSPHODIESTERASE 4A, cAMP-SPECIFIC; PDE4A *600127 : PHOSPHODIESTERASE 4B, cAMP-SPECIFIC; PDE4B *600128 : PHOSPHODIESTERASE 4C, cAMP-SPECIFIC; PDE4C *600129 : PHOSPHODIESTERASE 4D, cAMP-SPECIFIC; PDE4D *600130 : APOLIPOPROTEIN B mRNA EDITING ENZYME, CATALYTIC POLYPEPTIDE 1; APOBEC1 *600131 : CHILDHOOD ABSENCE EPILEPSY; CAE #600132 : RETINITIS PIGMENTOSA 14; RP14 *600133 : LAMININ, ALPHA-4; LAMA4 ^600134 : MOVED TO 605158 *600135 : CORTEXIN; CTXN *600136 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 9; MAP3K9 *600137 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 10; MAP3K10 #600138 : RETINITIS PIGMENTOSA 11; RP11 600139 : SUBEPENDYMOMA *600140 : CREB-BINDING PROTEIN; CREBBP *600141 : HEAT-SHOCK 10-KD PROTEIN; HSPE1 600142 : CEREBROVASCULAR DISEASE WITH THIN SKIN, ALOPECIA, AND DISK DISEASE *600143 : EPILEPSY, PROGRESSIVE, WITH MENTAL RETARDATION; EPMR *600144 : INOSITOL 1,4,5-TRIPHOSPHATE RECEPTOR, TYPE 2; ITPR2 *600145 : SACRAL DEFECT WITH ANTERIOR MENINGOCELE; SDAM 600146 : SPASTIC PARAPLEGIA 5B, AUTOSOMAL RECESSIVE; SPG5B *600147 : MESENCHYME HOMEO BOX 1; MEOX1 600148 : GLYCEROL KINASE, TESTICULAR, TYPE A #600149 : GLYCEROL KINASE, TESTICULAR, TYPE B *600150 : POTASSIUM CHANNEL, CALCIUM-ACTIVATED, LARGE CONDUCTANCE, SUBFAMILY M, ALPHA MEMBER 1; KCNMA1 *600151 : BARDET-BIEDL SYNDROME 3; BBS3 *600152 : SEC13-RELATED GENE *600153 : PHOSPHATIDYLINOSITOL GLYCAN, CLASS F; PIGF *600154 : PHOSPHATIDYLINOSITOL GLYCAN, CLASS H; PIGH #600155 : HIRSCHSPRUNG DISEASE 2; HSCR2 *600156 : HIRSCHSPRUNG DISEASE 3 *600157 : ADAPTOR-RELATED PROTEIN COMPLEX 1, BETA-1 SUBUNIT; AP1B1 ^600158 : MOVED TO 251290 600159 : PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES *600160 : CYCLIN-DEPENDENT KINASE INHIBITOR 2A; CDKN2A *600161 : PRADER-WILLI/ANGELMAN REGION 1 *600162 : PRADER-WILLI/ANGELMAN REGION 5 *600163 : SODIUM CHANNEL, VOLTAGE-GATED, TYPE V, ALPHA SUBUNIT; SCN5A *600164 : GTP-BINDING MITOGEN-INDUCED T-CELL PROTEIN; GEM *600165 : NANOPHTHALMOS 1; NNO1 600166 : HYPERPARATHYROIDISM, PRIMARY, CAUSED BY WATER CLEAR CELL HYPERPLASIA *600167 : HISTAMINE RECEPTOR H1; HRH1 *600168 : MACROPHAGE STIMULATING 1 RECEPTOR; MST1R *600169 : MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I CHAIN-RELATED GENE A; MICA *600170 : AQUAPORIN 3; AQP3 600171 : GONADAL AGENESIS *600172 : METAL-REGULATORY TRANSCRIPTION FACTOR 1; MTF1 *600173 : JANUS KINASE 3; JAK3 *600174 : PHOSPHATIDYLINOSITOL TRANSFER PROTEIN; PITPN *600175 : SPINAL MUSCULAR ATROPHY, CONGENITAL NONPROGRESSIVE, OF LOWER LIMBS 600176 : PACHYGYRIA WITH MENTAL RETARDATION AND SEIZURES ^600177 : MOVED TO 300102 *600178 : MICROTUBULE-ASSOCIATED PROTEIN 1A; MAP1A *600179 : GUANYLATE CYCLASE 2D, MEMBRANE; GUCY2D ^600180 : MOVED TO 108355 *600181 : LIPOCALIN 2; LCN2 *600182 : SOLUTE CARRIER FAMILY 7, MEMBER 5; SLC7A5 *600183 : DUAL-SPECIFICITY PHOSPHATASE 3; DUSP3 *600184 : CARNITINE ACETYLTRANSFERASE; CRAT *600185 : BREAST CANCER 2, EARLY-ONSET; BRCA2 ^600186 : MOVED TO 300016 *600187 : EUKARYOTIC TRANSLATION INITIATION FACTOR 5A; EIF5A *600188 : AMINO-TERMINAL ENHANCER OF SPLIT; AES *600189 : TRANSDUCIN-LIKE ENHANCER OF SPLIT 1; TLE1 *600190 : TRANSDUCIN-LIKE ENHANCER OF SPLIT 3; TLE3 ^600191 : MOVED TO 300018 *600192 : SYNOVIAL SARCOMA TRANSLOCATION, CHROMOSOME 18; SS18 *600193 : WAARDENBURG SYNDROME, TYPE IIB; WS2B *600194 : KERATIN 2A; KRT2A #600195 : VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL; VMCM ^600196 : MOVED TO 300019 *600197 : V-MAF AVIAN MUSCULOAPONEUROTIC FIBROSARCOMA ONCOGENE FAMILY, PROTEIN K; MAFK ^600198 : MOVED TO 163260 ^600199 : MOVED TO 300021 *600200 : EUKARYOTIC TRANSLATION INITIATION FACTOR 4E-LIKE 2; EIF4EL2 *600201 : AGOUTI SIGNALING PROTEIN; ASIP *600202 : DYSLEXIA, SPECIFIC, 2; DYX2 ^600203 : MOVED TO 300030 #600204 : EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2 ^600205 : MOVED TO 107748 *600206 : EPIDERMAL GROWTH FACTOR RECEPTOR PATHWAY SUBSTRATE 8; EPS8 *600207 : HIPPOCALCIN-LIKE 1; HPCAL1 600208 : MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS *600209 : EXOSTOSES, MULTIPLE, TYPE III; EXT3 *600210 : RUNT-RELATED TRANSCRIPTION FACTOR 3; RUNX3 *600211 : RUNT-RELATED TRANSCRIPTION FACTOR 2; RUNX2 *600212 : FATTY ACID SYNTHASE; FASN ^600213 : MOVED TO 176310 *600214 : ADVANCED GLYCOSYLATION END PRODUCT-SPECIFIC RECEPTOR; AGER *600215 : MICROFIBRILLAR-ASSOCIATED PROTEIN 1; MFAP1 ^600216 : MOVED TO 314700 ^600217 : MOVED TO 601545 ^600218 : MOVED TO 600068 ^600219 : MOVED TO 600069 *600220 : PHOSPHOLIPASE C, GAMMA-2; PLCG2 *600221 : TEK TYROSINE KINASE, ENDOTHELIAL; TEK *600222 : TYROSINE KINASE WITH IMMUNOGLOBULIN AND EGF FACTOR HOMOLOGY DOMAINS; TIE *600223 : SPINOCEREBELLAR ATAXIA 4; SCA4 *600224 : SPINOCEREBELLAR ATAXIA 5; SCA5 *600225 : GTP CYCLOHYDROLASE I; GCH1 ^600226 : MOVED TO 300031 *600227 : CYCLIN F; CCNF *600228 : SODIUM CHANNEL, NONVOLTAGE-GATED 1, ALPHA SUBUNIT; SCNN1A *600229 : SOLUTE CARRIER FAMILY 1 (GLUTAMATE/NEUTRAL AMINO ACID TRANSPORTER), MEMBER 4; SLC1A4 *600230 : PHOSPHOLIPASE C, BETA-3; PLCB3 *600231 : PALMOPLANTAR KERATODERMA, BOTHNIAN TYPE; PPKB *600232 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, BETA-2; GABRB2 *600233 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, GAMMA-3; GABRG3 *600234 : 3-@HYDROXY-3-METHYLGLUTARYL-CoA SYNTHASE 2, MITOCHONDRIAL; HMGCS2 *600235 : SODIUM CHANNEL, VOLTAGE-GATED, TYPE I, BETA SUBUNIT; SCN1B *600236 : CENTROMERIC PROTEIN F; CENPF *600237 : HISTONE CELL CYCLE REGULATION DEFECTIVE, S. CEREVISIAE, HOMOLOG OF, A; HIRA *600238 : TRANSGLUTAMINASE 3; TGM3 *600239 : G PROTEIN-COUPLED RECEPTOR 1; GPR1 *600240 : G PROTEIN-COUPLED RECEPTOR 2; GPR2 *600241 : G PROTEIN-COUPLED RECEPTOR 3; GPR3 *600242 : CHEMOKINE (C-C) RECEPTOR 7; CCR7 *600243 : DEFENDER AGAINST CELL DEATH; DAD1 *600244 : PROGRAMMED CELL DEATH 1; PDCD1 *600245 : FIBROMODULIN; FMOD *600246 : ELK4, ETS-DOMAIN PROTEIN; ELK4 *600247 : ELK3, ETS-DOMAIN PROTEIN; ELK3 ^600248 : MOVED TO 300009 *600249 : 10-@FORMYLTETRAHYDROFOLATE DEHYDROGENASE; FTHFD *600250 : SMALL INDUCIBLE CYTOKINE SUBFAMILY C, MEMBER 1; SCYC1 600251 : OCULOMAXILLOFACIAL DYSPLASIA WITH OBLIQUE FACIAL CLEFTS 600252 : LOWRY-MACLEAN SYNDROME *600253 : ARYL HYDROCARBON RECEPTOR; AHR ^600254 : MOVED TO 300032 ^600255 : MOVED TO 400000 *600256 : HYDROCEPHALUS, AUTOSOMAL DOMINANT #600257 : BOR-DUANE HYDROCEPHALUS CONTIGUOUS GENE SYNDROME *600258 : POSTMEIOTIC SEGREGATION INCREASED, S. CEREVISIAE, 1; PMS1 *600259 : POSTMEIOTIC SEGREGATION INCREASED, S. CEREVISIAE, 2; PMS2 ^600260 : MOVED TO 300008 ^600261 : REMOVED FROM DATABASE *600262 : PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 2; PTGS2 600263 : HELICOBACTER PYLORI INFECTION, SUSCEPTIBILITY TO *600264 : ARGININE VASOPRESSIN RECEPTOR 1B; AVPR1B ^600265 : MOVED TO 300033 *600266 : SOLUTE CARRIER FAMILY 11 (PROTON-COUPLED DIVALENT METAL ION TRANSPORTER), MEMBER 1; SLC11A1 *600267 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 13; PTPN13 600268 : APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS 600269 : SHORT TARSUS WITH ABSENCE OF LOWER EYELASHES; STALE *600270 : PROCOLLAGEN C-ENDOPEPTIDASE ENHANCER; PCOLCE *600271 : DESMOCOLLIN 3; DSC3 *600272 : COILIN; COIL #600273 : POLYCYSTIC KIDNEY DISEASE, INFANTILE SEVERE, WITH TUBEROUS SCLEROSIS; PKDTS #600274 : FRONTOTEMPORAL DEMENTIA *600275 : NOTCH, DROSOPHILA, HOMOLOG OF, 2; NOTCH2 *600276 : NOTCH, DROSOPHILA, HOMOLOG OF, 3; NOTCH3 *600277 : INHIBITOR OF DNA BINDING 3; ID3 *600278 : RAP1, GTPase-ACTIVATING PROTEIN 1; RAP1GA1 *600279 : PEROXISOMAL FARNESYLATED PROTEIN; PXF *600280 : NUCLEOTIDE-BINDING PROTEIN 1; NUBP1 *600281 : HEPATOCYTE NUCLEAR FACTOR 4-ALPHA; HNF4A *600282 : GLUTAMATE RECEPTOR, IONOTROPIC, KAINATE 4; GRIK4 *600283 : GLUTAMATE RECEPTOR, IONOTROPIC, KAINATE 5; GRIK5 *600284 : ELEVEN NINETEEN LYSINE-RICH LEUKEMIA GENE *600285 : EUKARYOTIC TRANSLATION TERMINATION FACTOR 1; ETF1 *600286 : PHOSPHATIDYLINOSITOL 4-KINASE, CATALYTIC, ALPHA; PIK4CA *600287 : GLYCYL-tRNA SYNTHETASE; GARS *600288 : HEPATOCYTE NUCLEAR FACTOR 3-BETA; HNF3B *600289 : MITOGEN-ACTIVATED PROTEIN KINASE 14; MAPK14 ^600290 : MOVED TO 600289 *600291 : ADENYLATE CYCLASE 3; ADCY3 *600292 : ADENYLATE CYCLASE 4; ADCY4 *600293 : ADENYLATE CYCLASE 5; ADCY5 *600294 : ADENYLATE CYCLASE 6; ADCY6 *600295 : NATRIURETIC PEPTIDE PRECURSOR B; NPPB *600296 : NATRIURETIC PEPTIDE PRECURSOR C; NPPC *600297 : CAUDAL-TYPE HOMEO BOX TRANSCRIPTION FACTOR 2; CDX2 *600298 : LIM HOMEO BOX TRANSCRIPTION FACTOR 1, ALPHA; LMX1A *600299 : PERICENTRIOLAR MATERIAL 1; PCM1 *600300 : SOLUTE CARRIER FAMILY 1 (GLIAL HIGH AFFINITY GLUTAMATE TRANSPORTER), MEMBER 2; SLC1A2 *600301 : ACYL-CoA DEHYDROGENASE, SHORT/BRANCHED CHAIN; ACADSB 600302 : MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIAL APPEARANCE *600303 : GUANINE NUCLEOTIDE-RELEASING FACTOR 2; GRF2 ^600304 : MOVED TO 170400 *600305 : DODECENOYL-CoA DELTA ISOMERASE; DCI *600306 : PROTEASOME SUBUNIT, BETA-TYPE, 5; PSMB5 *600307 : PROTEASOME SUBUNIT, BETA-TYPE, 6; PSMB6 *600308 : AQUAPORIN 4; AQP4 #600309 : ATRIOVENTRICULAR SEPTAL DEFECT; AVSD *600310 : CARTILAGE OLIGOMERIC MATRIX PROTEIN; COMP *600311 : GRANZYME M; GZMM *600312 : NUCLEOSIDE DIPHOSPHATE-LINKED MOIETY X MOTIF, 1; NUDT1 ^600313 : MOVED TO 600535 *600314 : SHB ADAPTOR PROTEIN; SHB *600315 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 4; TNFRSF4 #600316 : DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 3; DFNB3 *600317 : TROPOMYOSIN 4; TPM4 *600318 : DIABETES MELLITUS, INSULIN-DEPENDENT, 3; IDDM3 *600319 : DIABETES MELLITUS, INSULIN-DEPENDENT, 4; IDDM4 *600320 : DIABETES MELLITUS, INSULIN-DEPENDENT, 5; IDDM5 *600321 : DIABETES MELLITUS, INSULIN-DEPENDENT, 7; IDDM7 *600322 : SYNAPTOSOMAL-ASSOCIATED PROTEIN, 25-KD; SNAP25 *600323 : REGULATOR OF G PROTEIN SIGNALING 1; RGS1 *600324 : SMALL INDUCIBLE CYTOKINE SUBFAMILY B, MEMBER 5; SCYB5 600325 : AMINOPTERIN SYNDROME SINE AMINOPTERIN *600326 : DEAD/H BOX 6; DDX6 *600327 : SYNAPTOTAGMIN 3; SYT3 *600328 : MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 6; MLLT6 600329 : OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY 600330 : SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME 600331 : PARC SYNDROME *600332 : RIPPLING MUSCLE DISEASE 1; RMD1 600333 : MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA *600334 : TIBIAL MUSCULAR DYSTROPHY, TARDIVE *600335 : SUCCINICACIDEMIA *600336 : SOLUTE CARRIER FAMILY 18, MEMBER 3; SLC18A3 *600337 : BRADYKININ RECEPTOR B1; BDKRB1 *600338 : ARYLACETAMIDE DEACETYLASE; AADAC ^600339 : MOVED TO 300043 *600340 : PLASMOLIPIN; PMLP *600341 : TYRO3 PROTEIN TYROSINE KINASE; TYRO3 *600342 : G PROTEIN-COUPLED RECEPTOR, RETINAL; RGR *600343 : PAROTID SALIVARY GLANDS, POLYCYSTIC DISEASE OF ^600344 : MOVED TO 300058 *600345 : BETACELLULIN; BTC *600346 : ZINC FINGER PROTEIN 144; ZNF144 600347 : BREVICAN 600348 : BAND HETEROTOPIA OF BRAIN *600349 : INHIBITOR OF DNA BINDING 1; ID1 ^600350 : MOVED TO 300034 600351 : ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY ^600352 : MOVED TO 112205 *600353 : S100 CALCIUM-BINDING PROTEIN A7; S100A7 *600354 : SURVIVAL OF MOTOR NEURON 1, TELOMERIC; SMN1 *600355 : BACULOVIRAL IAP REPEAT-CONTAINING PROTEIN 1; BIRC1 600356 : PACHYDERMODACTYLY, FAMILIAL *600357 : RIBOSOMAL PROTEIN S8; RPS8 *600358 : GUANINE MONOPHOSPHATE SYNTHETASE; GMPS *600359 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 1; KCNJ1 *600360 : APLASIA CUTIS CONGENITA OF LIMBS, RECESSIVE *600361 : PERONEAL MUSCULAR ATROPHY WITH PYRAMIDAL FEATURES *600362 : FLIGHTLESS I, DROSOPHILA, HOMOLOG OF; FLII *600363 : SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT; SPG6 *600364 : GUANYLATE CYCLASE ACTIVATOR 1A; GUCA1A *600365 : ACTIVE BCR-RELATED GENE; ABR *600366 : ISL1 TRANSCRIPTION FACTOR, LIM/HOMEODOMAIN; ISL1 *600367 : CLEAVAGE STIMULATION FACTOR, 3-PRIME PRE-RNA, SUBUNIT 3, 77-KD; CSTF3 *600368 : CLEAVAGE STIMULATION FACTOR, 3-PRIME PRE-RNA, SUBUNIT 2, 64-KD; CSTF2 *600369 : CLEAVAGE STIMULATION FACTOR, 3-PRIME PRE-RNA, SUBUNIT 1, 50-KD; CSTF1 *600370 : SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER), MEMBER 3; SLC25A3 ^600371 : MOVED TO 142695 *600372 : NEURAL PRECURSOR CELL EXPRESSED, DEVELOPMENTALLY DOWNREGULATED 1; NEDD1 600373 : CODAS SYNDROME *600374 : BBS4 GENE; BBS4 *600375 : X-RAY REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 2; XRCC2 #600376 : OSLER-RENDU-WEBER SYNDROME 2; ORW2 *600377 : GALANIN RECEPTOR 1; GALR1 *600378 : INNER MEMBRANE PROTEIN, MITOCHONDRIAL; IMMT *600379 : MYELIN TRANSCRIPTION FACTOR 1; MYT1 *600380 : NUCLEAR RECEPTOR SUBFAMILY 1, GROUP H, MEMBER 2; NR1H2 *600381 : KINECTIN; KTN1 *600382 : MYC PROMOTER-BINDING PROTEIN *600383 : MESOMELIA-SYNOSTOSES SYNDROME *600384 : APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSAL IV *600385 : ADENYLATE CYCLASE 7; ADCY7 *600386 : INHIBITOR OF DNA BINDING 2; ID2 *600387 : BONE MARROW STROMAL CELL ANTIGEN 1; BST1 *600388 : MEPRIN, ALPHA SUBUNIT; MEP1A *600389 : MEPRIN, BETA SUBUNIT; MEP1B *600390 : UPSTREAM STIMULATORY FACTOR 2; USF2 *600391 : GLUCOSAMINYL (N-ACETYL) TRANSFERASE 1, CORE 2; GCNT1 *600392 : RAD52, YEAST, HOMOLOG OF; RAD52 *600393 : FLAP STRUCTURE-SPECIFIC ENDONUCLEASE 1; FEN1 ^600394 : MOVED TO 300036 *600395 : GLYPICAN 1; GPC1 *600396 : DEAD/H BOX 8; DDX8 *600397 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAB-RELATED SUBFAMILY, MEMBER 1; KCNB1 *600398 : ZINC FINGER PROTEIN 160; ZNF160 *600399 : PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, DYSPLASTIC NAILS *600400 : PROLYL ENDOPEPTIDASE; PREP ^600401 : MOVED TO 600247 ^600402 : MOVED TO 300035 *600403 : FIBROBLAST ACTIVATION PROTEIN, ALPHA; FAP *600404 : REPLICATION FACTOR C, SUBUNIT 2; RFC2 *600405 : REPLICATION FACTOR C, SUBUNIT 3; RFC3 ^600406 : MOVED TO 102577 *600407 : REPLICATION FACTOR C, SUBUNIT 5; RFC5 *600408 : DISCOIDIN DOMAIN RECEPTOR FAMILY, MEMBER 1; DDR1 *600409 : PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-DELTA; PPARD *600410 : TUMOR NECROSIS FACTOR-ALPHA-INDUCED PROTEIN 6; TNFAIP6 *600411 : GUANYLATE BINDING PROTEIN 1, INTERFERON-INDUCIBLE, 67-KD; GBP1 *600412 : GUANYLATE BINDING PROTEIN 2, INTERFERON-INDUCIBLE; GBP2 *600413 : GUANYLATE BINDING PROTEIN 3; GBP3 *600414 : PEROXISOME RECEPTOR 1; PXR1 *600415 : TOCOPHEROL TRANSFER PROTEIN, ALPHA; TTPA 600416 : MUSCULAR DYSTROPHY, SCAPULOHUMERAL *600417 : NUCLEOTIDASE, 5-PRIME, CYTOSOLIC II, NT5C2 *600418 : AMPHIPHYSIN; AMPH 600419 : ANGIOKERATOMA CORPORIS DIFFUSUM WITH ARTERIOVENOUS FISTULAS ^600420 : MOVED TO 300039 *600421 : GLYCINE RECEPTOR, ALPHA-3 SUBUNIT; GLRA3 *600422 : FATTY ACID-BINDING PROTEIN 6; FABP6 *600423 : ENDOTHELIN-CONVERTING ENZYME 1; ECE1 *600424 : SOLUTE CARRIER FAMILY 19, MEMBER 1; SLC19A1 ^600425 : MOVED TO 189902 *600426 : E2F TRANSCRIPTION FACTOR 2; E2F2 *600427 : E2F TRANSCRIPTION FACTOR 3; E2F3 *600428 : VAV2 ONCOGENE; VAV2 *600429 : GLUCOSAMINYL (N-ACETYL) TRANSFERASE 2, I-BRANCHING ENZYME; GCNT2 *600430 : BRACHYDACTYLY-MENTAL RETARDATION SYNDROME *600431 : CYCLIN-DEPENDENT KINASE INHIBITOR 2B; CDKN2B *600432 : CEREBELLIN 1 PRECURSOR; CBLN1 *600433 : CEREBELLIN 2 PRECURSOR; CBLN2 *600434 : FATTY ACID-BINDING PROTEIN 4; FABP4 *600435 : CARDIOTROPHIN 1; CTF1 *600436 : GLUTATHIONE S-TRANSFERASE, THETA-1; GSTT1 *600437 : GLUTATHIONE S-TRANSFERASE, THETA-2; GSTT2 *600438 : TRANSCRIPTION FACTOR A, MITOCHONDRIAL; TFAM *600439 : SINGLE-STRANDED DNA-BINDING PROTEIN; SSBP *600440 : ENDONUCLEASE G, MITOCHONDRIAL; ENDOG *600441 : GROWTH ARREST-SPECIFIC 6; GAS6 *600442 : AQUAPORIN 5; AQP5 *600443 : GLUTAREDOXIN; GLRX *600444 : SOLUTE CARRIER FAMILY 5 (INOSITOL TRANSPORTER), MEMBER 3; SLC5A3 *600445 : ADENOSINE A3 RECEPTOR; ADORA3 *600446 : ADENOSINE A2B RECEPTOR; ADORA2B *600447 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 12; MAP3K12 *600448 : PROTEIN KINASE C, THETA FORM; PRKCQ *600449 : ALDO-KETO REDUCTASE FAMILY 1, MEMBER 1; AKR1C1 *600450 : ALDO-KETO REDUCTASE FAMILY 1, MEMBER C2; AKR1C2 *600451 : ALDO-KETO REDUCTASE FAMILY 1, MEMBER C4; AKR1C4 ^600452 : MOVED TO 600408 *600453 : ZINC FINGER PROTEIN 147; ZNF147 *600454 : RIBOSOMAL PROTEIN S3; RPS3 #600455 : RNA, U15A SMALL NUCLEOLAR; RNU15A *600456 : NEUROTROPHIC TYROSINE KINASE, RECEPTOR, TYPE 2; NTRK2 600457 : HYPERTRICHOSIS, ANTERIOR CERVICAL 600458 : ADENOMYOSIS 600459 : ARTERIAL DISSECTION WITH LENTIGINOSIS 600460 : CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY 600461 : HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES 600462 : MYOPATHY WITH LACTIC ACIDOSIS AND SIDEROBLASTIC ANEMIA *600463 : ALDEHYDE DEHYDROGENASE 1 FAMILY, MEMBER A3; ALDH1A3 *600464 : ADP-RIBOSYLATION FACTOR 6; ARF6 *600465 : ANKYRIN 3; ANK3 *600466 : ALDEHYDE DEHYDROGENASE 3 FAMILY, MEMBER B1; ALDH3B1 *600467 : MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 4; MHS4 ^600468 : MOVED TO 300011 *600469 : NUCLEAR CAP-BINDING PROTEIN 1; NCBP1 *600470 : ZINC FINGER PROTEIN OF CEREBELLUM, 1; ZIC1 *600471 : DEFENSIN, ALPHA, 6; DEFA6 *600472 : DEFENSIN, ALPHA, 5; DEFA5 *600473 : PURINE-RICH ELEMENT-BINDING PROTEIN A; PURA *600474 : CATHELICIDIN ANTIMICROBIAL PEPTIDE; CAMP *600475 : TAF10 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 30-KD; TAF10 ^600476 : MOVED TO 300040 *600477 : SOLUTE CARRIER FAMILY 9, ISOFORM A5; SLC9A5 *600478 : SUPERKILLER VIRALICIDIC ACTIVITY 2, S. CEREVISIAE, HOMOLOG-LIKE; SKIV2L ^600479 : MOVED TO 120324 *600480 : TRANSCRIPTION FACTOR 12; TCF12 *600481 : STEROL REGULATORY ELEMENT-BINDING TRANSCRIPTION FACTOR 2; SREBF2 ^600482 : MOVED TO 300116 *600483 : FIBROBLAST GROWTH FACTOR 8; FGF8 ^600484 : MOVED TO 300002 ^600485 : MOVED TO 300003 ^600486 : MOVED TO 300076 *600487 : PROPROTEIN CONVERTASE, SUBTILISIN/KEXIN-TYPE, 4; PCSK4 *600488 : PROPROTEIN CONVERTASE, SUBTILISIN/KEXIN-TYPE, 5; PCSK5 *600489 : NUCLEAR FACTOR OF ACTIVATED T CELLS, CYTOPLASMIC, CALCINEURIN-DEPENDENT 1; NFATC1 *600490 : NUCLEAR FACTOR OF ACTIVATED T CELLS, CYTOPLASMIC, CALCINEURIN-DEPENDENT 2; NFATC2 *600491 : MICROFIBRIL-ASSOCIATED PROTEIN 3; MFAP3 *600492 : NUCLEAR FACTOR ERYTHROID 2-LIKE 2; NFE2L2 *600493 : EGF-LIKE MODULE-CONTAINING, MUCIN-LIKE HORMONE RECEPTOR 1; EMR1 *600494 : POU DOMAIN, CLASS 3, TRANSCRIPTION FACTOR 2; POU3F2 *600495 : EUKARYOTIC TRANSLATION INITIATION FACTOR 4-GAMMA, 1; EIF4G1 #600496 : MATURITY-ONSET DIABETES OF THE YOUNG, TYPE III; MODY3 *600497 : PROTEIN KINASE, AMP-ACTIVATED, CATALYTIC, ALPHA-2; PRKAA2 *600498 : MIC2-RELATED GENE; MIC2R ^600499 : REMOVED FROM DATABASE ^600500 : MOVED TO 600758 #600501 : ABCD SYNDROME *600502 : IMMUNOGLOBULIN MU BINDING PROTEIN 2; IGHMBP2 *600503 : ACTIVATED RNA POLYMERASE II TRANSCRIPTION COFACTOR 4 *600504 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 4; KCNJ4 *600505 : CASEIN KINASE I, ALPHA-1; CSNK1A1 ^600506 : MOVED TO 604286 *600507 : ADP-RIBOSYLATION FACTOR 2; ARF2 *600508 : NCK ADAPTOR PROTEIN 1; NCK1 *600509 : ATP-BINDING CASSETTE, SUBFAMILY C, MEMBER 8; ABCC8 *600510 : GLAUCOMA-RELATED PIGMENT DISPERSION SYNDROME; GPDS1 600511 : SCHIZOPHRENIA 3; SCZD3 #600512 : EPILEPSY, PARTIAL, WITH AUDITORY FEATURES; ADPEAF #600513 : EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 1 *600514 : REELIN; RELN *600515 : PURINERGIC RECEPTOR P2Y, G PROTEIN-COUPLED, 12 *600516 : BCL2 ANTAGONIST KILLER 1; BAK1 *600517 : SQUAMOUS CELL CARCINOMA ANTIGEN 1; SCCA1 *600518 : SQUAMOUS CELL CARCINOMA ANTIGEN 2; SCCA2 *600519 : GENERAL TRANSCRIPTION FACTOR IIA, GAMMA SUBUNIT; GTF2A2 *600520 : GENERAL TRANSCRIPTION FACTOR IIA, ALPHA/BETA SUBUNITS; GTF2A1 *600521 : MANNAN-BINDING LECTIN SERINE PROTEASE 1; MASP1 *600522 : PHOSPHOLIPASE A2, GROUP IVA; PLA2G4A *600523 : SOLUTE CARRIER FAMILY 11 (PROTON-COUPLED DIVALENT METAL ION TRANSPORTER), MEMBER 2; SLC11A2 *600524 : RYK RECEPTOR-LIKE TYROSINE KINASE; RYK *600525 : DISTAL-LESS HOMEO BOX 3; DLX3 *600526 : ELKL MOTIF KINASE; EMK1 *600527 : EPHRIN B2; EFNB2 *600528 : CARNITINE PALMITOYLTRANSFERASE I, LIVER; CPT1A *600529 : AU-SPECIFIC RNA-BINDING PROTEIN; AUH *600530 : SOLUTE CARRIER FAMILY 9, ISOFORM A2; SLC9A2 *600531 : SOLUTE CARRIER FAMILY 9, ISOFORM A4; SLC9A4 *600532 : NADH-UBIQUINONE OXIDOREDUCTASE FLAVOPROTEIN 2; NDUFV2 *600533 : VANG-LIKE 2; VANGL2 *600534 : BONE MARROW STROMAL CELL ANTIGEN 2; BST2 *600535 : MESENCHYME HOMEO BOX 2; MEOX2 *600536 : INTEGRIN, ALPHA-7; ITGA7 *600537 : RECQ PROTEIN-LIKE; RECQL *600538 : PEROXIREDOXIN 2; PRDX2 ^600539 : MOVED TO 300094 *600540 : TRANSCRIPTION FACTOR Sp4; SP4 *600541 : ETS VARIANT GENE 1; ETV1 *600542 : NUCLEAR RECEPTOR SUBFAMILY 4, GROUP A, MEMBER 3; NR4A3 *600543 : V-ERB-B2 AVIAN ERYTHROBLASTIC LEUKEMIA VIRAL ONCOGENE HOMOLOG 4; ERBB4 *600544 : SOLUTE CARRIER FAMILY 15 (OLIGOPEPTIDE TRANSPORTER), MEMBER 1; SLC15A1 ^600545 : MOVED TO 300240 600546 : INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY *600547 : CYSTEINE CONJUGATE BETA-LYASE *600548 : HEAT-SHOCK 70-KD PROTEIN 9B; HSPA9B *600549 : IK CYTOKINE, DOWNREGULATOR OF HLA II; IK *600550 : CATHEPSIN O; CTSO *600551 : G PROTEIN-COUPLED RECEPTOR 4; GPR4 *600552 : CHEMOKINE (C) XC RECEPTOR 1; CCXCR1 *600553 : G PROTEIN-COUPLED RECEPTOR 6; GPR6 *600554 : INTERLEUKIN 15; IL15 *600555 : SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 1; STAT1 *600556 : SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 2; STAT2 ^600557 : MOVED TO 102582 *600558 : SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 4; STAT4 600559 : HYDROCEPHALUS, ENDOCARDIAL FIBROELASTOSIS, AND CATARACTS *600560 : SHC TRANSFORMING PROTEIN; SHC1 600561 : SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY *600562 : CADHERIN 12; CDH12 *600563 : PROSTAGLANDIN F RECEPTOR; PTGFR *600564 : INTER-ALPHA-TRYPSIN INHIBITOR, HEAVY CHAIN 4; ITIH4 *600565 : NEUREXIN 1; NRXN1 *600566 : NEUREXIN 2; NRXN2 *600567 : NEUREXIN 3; NRXN3 *600568 : NEUROLIGIN 1; NLGN1 ^600569 : MOVED TO 300103 *600570 : CHLORIDE CHANNEL 2; CLCN2 *600571 : RE1-SILENCING TRANSCRIPTION FACTOR; REST *600572 : SPLICING FACTOR, ARGININE/SERINE-RICH, 7; SFRS7 *600573 : TAF7 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 55-KD; TAF7 *600574 : LEUCINE ZIPPER-LIKE TRANSCRIPTIONAL REGULATOR 1; LZTR1 *600575 : TRANSLIN; TSN *600576 : GATA-BINDING PROTEIN 4; GATA4 *600577 : LIM HOMEO BOX GENE 3; LHX3 *600578 : OLFACTORY RECEPTOR, FAMILY 2, SUBFAMILY H, MEMBER 3; OR2H3 *600579 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, O; PTPRO *600580 : CHLORIDE CHANNEL 3; CLCN3 *600581 : INHIBITOR OF DNA BINDING 4; ID4 *600582 : ASPARTATE BETA-HYDROXYLASE; ASPH *600583 : TEC PROTEIN TYROSINE KINASE; TEC *600584 : CARDIAC-SPECIFIC HOMEO BOX; CSX *600585 : TRANSGLUTAMINASE 4; TGM4 *600586 : EPITHELIAL CELL TRANSFORMING SEQUENCE 2 ONCOGENE; ECT2 *600587 : POM121/ZP3 FUSION PROTEIN; POMZP3 600588 : THROMBOCYTOPENIA, CONGENITAL DYSMEGAKARYOPOIETIC, PARIS-TROUSSEAU TYPE *600589 : SERUM RESPONSE FACTOR; SRF *600590 : PROTEIN PHOSPHATASE 1, CATALYTIC SUBUNIT, BETA ISOFORM; PPP1CB *600591 : SMALL NUCLEAR RNA-ACTIVATING PROTEIN COMPLEX, POLYPEPTIDE 1; SNAPC1 *600592 : MINICHROMOSOME MAINTENANCE, S. CEREVISIAE, HOMOLOG OF, 7; MCM7 *600593 : CRANIOSYNOSTOSIS, ADELAIDE TYPE; CRSA *600594 : DIGEORGE CRITICAL REGION GENE 2 *600595 : POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE *600596 : MICROFIBRIL-ASSOCIATED PROTEIN 4; MFAP4 *600597 : PHOSPHOLIPASE C-LIKE 1; PLCL1 600598 : SETTING-SUN PHENOMENON, FAMILIAL BENIGN *600599 : KRUPPEL-LIKE FACTOR 1; KLF1 *600600 : EPHRIN RECEPTOR EphB1; EPHB1 ^600601 : MOVED TO 600289 ^600602 : MOVED TO 300083 ^600603 : MOVED TO 300071 ^600604 : MOVED TO 600376 *600605 : METAXIN 1; MTX1 ^600606 : REMOVED FROM DATABASE *600607 : TRANSCRIPTION FACTOR-LIKE 1; TCFL1 *600608 : PROCOLLAGEN-PROLINE,2-OXOGLUTARATE-4-DIOXYGENASE, ALPHA SUBUNIT, ISOFORM 2; P4HA2 *600609 : GA-BINDING PROTEIN TRANSCRIPTION FACTOR, ALPHA SUBUNIT; GABPA *600610 : GA-BINDING PROTEIN TRANSCRIPTION FACTOR, BETA SUBUNIT 1; GABPB1 *600611 : FK506-BINDING PROTEIN 4; FKBP4 ^600612 : MOVED TO 300101 *600613 : NEUROBLASTOMA CANDIDATE REGION, SUPPRESSION OF TUMORIGENICITY 1; NBL1 *600614 : S100 CALCIUM-BINDING PROTEIN P; S100P *600615 : LECTIN, GALACTOSIDE-BINDING, SOLUBLE, 7; LGALS7 *600616 : LUMICAN; LUM *600617 : STEROIDOGENIC ACUTE REGULATORY PROTEIN; STAR *600618 : ETS VARIANT GENE 6; ETV6 ^600619 : MOVED TO 300097 *600620 : FK506-BINDING PROTEIN 1B; FKBP1B *600621 : STATHMIN-LIKE 2; STMN2 ^600622 : MOVED TO 300069 *600623 : KANGAI 1; KAI1 *600624 : CONE-ROD DYSTROPHY 1; CORD1 600625 : CLEFT LIP, CONGENITAL HEALED *600626 : LECTIN, GALACTOSIDE-BINDING, SOLUBLE, 3 BINDING PROTEIN; LGALS3BP 600627 : HYPERTRYPTOPHANEMIA, FAMILIAL 600628 : LOOSE ANAGEN HAIR SYNDROME *600629 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DO BETA; HLA-DOB *600630 : UV-SENSITIVE SYNDROME; UVS *600631 : ENURESIS, NOCTURNAL, 1; ENUR1 *600632 : OPIOID-BINDING PROTEIN/CELL ADHESION MOLECULE-LIKE; OPCML *600633 : TREFOIL FACTOR 3; TFF3 600634 : PROLACTINOMA, FAMILIAL *600635 : THYROID TRANSCRIPTION FACTOR 1; TITF1 *600636 : CASPASE 3, APOPTOSIS-RELATED CYSTEINE PROTEASE; CASP3 *600637 : SOLUTE CARRIER FAMILY 1 (HIGH AFFINITY ASPARTATE/GLUTAMATE TRANSPORTER), MEMBER 6; SLC1A6 *600638 : FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3; FEOM3 *600639 : CASPASE 2, APOPTOSIS-RELATED CYSTEINE PROTEASE; CASP2 ^600640 : MOVED TO 311770 *600641 : SULFOTRANSFERASE FAMILY 1A, PHENOL-PREFERRING, MEMBER 3; SULT1A3 *600642 : MINOR HISTOCOMPATIBILITY ANTIGEN HA-2 600643 : CAROLI DISEASE, ISOLATED *600644 : POLIOVIRUS RECEPTOR-LIKE 1; PVRL1 ^600645 : MOVED TO 600579 *600646 : PROTEIN C RECEPTOR; PROCR *600647 : HOMEO BOX (H6 FAMILY) 2; HMX2 #600648 : NEVUS, EPIDERMAL, EPIDERMOLYTIC HYPERKERATOTIC TYPE #600649 : HYPOGLYCEMIA, HYPOKETOTIC, WITH DEFICIENCY OF CARNITINE PALMITOYLTRANSFERASE II *600650 : CARNITINE PALMITOYLTRANSFERASE II; CPT2 #600651 : FRAGILE SITE 11B; FRA11B *600652 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 4; DFNA4 ^600653 : MOVED TO 600381 *600654 : PROTEASOME ACTIVATOR SUBUNIT 1; PSME1 *600655 : EUKARYOTIC TRANSLATION ELONGATION FACTOR 1, BETA-2; EEF1B2 *600656 : EUKARYOTIC TRANSLATION ELONGATION FACTOR 1, BETA-3; EEF1B3 ^600657 : MOVED TO 300140 *600658 : PROTEIN PHOSPHATASE 5, CATALYTIC SUBUNIT; PPP5C *600659 : E2F TRANSCRIPTION FACTOR 4; E2F4 *600660 : MADS BOX TRANSCRIPTION ENHANCER FACTOR 2, POLYPEPTIDE A; MEF2A *600661 : MADS BOX TRANSCRIPTION ENHANCER FACTOR 2, POLYPEPTIDE B; MEF2B *600662 : MADS BOX TRANSCRIPTION ENHANCER FACTOR 2, POLYPEPTIDE C; MEF2C *600663 : MADS BOX TRANSCRIPTION ENHANCER FACTOR 2, POLYPEPTIDE D; MEF2D *600664 : CONSERVED HELIX-LOOP-HELIX UBIQUITOUS KINASE; CHUK *600665 : MELATONIN RECEPTOR 1A; MTNR1A 600666 : POLYCYSTIC KIDNEY DISEASE 3, AUTOSOMAL DOMINANT; PKD3 *600667 : FRIZZLED, DROSOPHILA, HOMOLOG OF, 2; FZD2 *600668 : CHONDROCALCINOSIS 1; CCAL1 #600669 : EPILEPSY, IDIOPATHIC GENERALIZED; IGE 600670 : VARICELLA, SEVERE RECURRENT ^600671 : MOVED TO 600594 ^600672 : MOVED TO 300025 *600673 : UPSTREAM BINDING TRANSCRIPTION FACTOR (RNA POLYMERASE I); UBTF *600674 : MICROTIA-ANOTIA *600675 : X-RAY REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 3; XRCC3 *600676 : CATR TUMORIGENIC CONVERSION 1; CATR1 ^600677 : MOVED TO 300192 *600678 : MutS, E. COLI, HOMOLOG OF, 6; MSH6 600679 : DERMOID CYSTS, FAMILIAL FRONTONASAL #600680 : CEROID LIPOFUSCINOSIS, JUVENILE NEURONAL, WITH GRANULAR OSMIOPHILIC DEPOSITS *600681 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 2; KCNJ2 *600682 : SOLUTE CARRIER FAMILY 16, MEMBER 1; SLC16A1 ^600683 : MOVED TO 109190 *600684 : T-LYMPHOCYTE SURFACE ANTIGEN LY-9; LY9 *600685 : KARYOPHERIN ALPHA-2; KPNA2 *600686 : KARYOPHERIN ALPHA-1; KPNA1 *600687 : T-CELL LYMPHOMA INVASION AND METASTASIS 1; TIAM1 *600688 : CARBOXYPEPTIDASE A2, PANCREATIC; CPA2 ^600689 : MOVED TO 300096 *600690 : T-CELL LEUKEMIA TRANSLOCATION-ASSOCIATED GENE; TCTA *600691 : SOLUTE CARRIER FAMILY 27, MEMBER 1; SLC27A1 *600692 : TROPONIN T3, FAST SKELETAL; TNNT3 *600693 : POLYPYRIMIDINE TRACT-BINDING PROTEIN 1; PTBP1 *600694 : INTERLEUKIN 6 SIGNAL TRANSDUCER; IL6ST *600695 : TRANSCRIPTION ELONGATION FACTOR B, 1-LIKE; TCEB1L *600696 : ENOYL-CoA HYDRATASE, PEROXISOMAL; ECH1 *600697 : RETINOBLASTOMA-BINDING PROTEIN 5; RBBP5 *600698 : HIGH MOBILITY GROUP PROTEIN ISOFORM I-C; HMGIC ^600699 : MOVED TO 400003 *600700 : LIM DOMAIN-CONTAINING PREFERRED TRANSLOCATION PARTNER IN LIPOMA; LPP *600701 : HIGH MOBILITY GROUP PROTEIN ISOFORMS I AND Y; HMGIY *600702 : SODIUM CHANNEL, VOLTAGE-GATED, TYPE VIII, ALPHA SUBUNIT; SCN8A *600703 : RIBOSOMAL PROTEIN S1-LIKE; RPS1L ^600704 : MOVED TO 300047 600705 : SATOYOSHI SYNDROME 600706 : PROXIMAL MYOPATHY WITH FOCAL DEPLETION OF MITOCHONDRIA *600707 : SIGNAL RECOGNITION PARTICLE, 9-KD; SRP9 *600708 : SIGNAL RECOGNITION PARTICLE, 14-KD; SRP14 *600709 : ISOLEUCYL-tRNA SYNTHETASE; IARS ^600710 : MOVED TO 600564 *600711 : ETS VARIANT GENE 4; ETV4 *600712 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN K; HNRNPK *600713 : 11-@BETA-HYDROXYSTEROID DEHYDROGENASE, TYPE I; HSD11B1 *600714 : DUAL-SPECIFICITY PHOSPHATASE 1; DUSP1 *600715 : THROMBOSPONDIN IV; THBS4 600716 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE 8; PTPN8 ^600717 : MOVED TO 120165 ^600718 : MOVED TO 185535 *600719 : NITRIC OXIDE SYNTHASE, MACROPHAGE, TYPE 2B; NOS2B *600720 : NITRIC OXIDE SYNTHASE, MACROPHAGE, TYPE 2C; NOS2C 600721 : D-2-@HYDROXYGLUTARICACIDURIA *600722 : PALMITOYL-PROTEIN THIOESTERASE 1; PPT1 *600723 : MEMBRANE PROTEIN, PALMITOYLATED 2; MPP2 *600724 : CYCLIC NUCLEOTIDE-GATED CHANNEL, BETA-1; CNGB1 *600725 : SONIC HEDGEHOG; SHH *600726 : INDIAN HEDGEHOG; IHH *600727 : NUCLEAR FACTOR I/A; NFIA *600728 : NUCLEAR FACTOR I/B; NFIB *600729 : NUCLEAR FACTOR I/C; NFIC *600730 : G PROTEIN-COUPLED RECEPTOR 7; GPR7 *600731 : G PROTEIN-COUPLED RECEPTOR 8; GPR8 *600732 : ADP-RIBOSYLATION FACTOR 4-LIKE; ARF4L *600733 : INSULIN PROMOTER FACTOR 1; IPF1 *600734 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 5; KCNJ5 *600735 : INTERFERON-INDUCED PROTEIN 35; IFI35 600736 : VELOFACIOSKELETAL SYNDROME #600737 : INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE; IBM2 *600738 : SELECTIN P LIGAND; SELPLG *600739 : SHC-LIKE PROTEIN; SHCL1 *600740 : HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III; HHC3 *600741 : PRIMASE POLYPEPTIDE 2B; PRIM2B *600742 : TRANSFORMING GROWTH FACTOR-BETA RECEPTOR, TYPE III; TGFBR3 *600743 : TRANSCRIPTION FACTOR AP4; TFAP4 *600744 : T-CELL TRANSCRIPTION FACTOR EB; TFEB *600745 : APOLIPOPROTEIN C-IV; APOC4 *600746 : CAUDAL-TYPE HOMEO BOX TRANSCRIPTION FACTOR 1; CDX1 *600747 : T-BOX 2; TBX2 *600748 : TESTIS ENHANCED GENE TRANSCRIPT; TEGT *600749 : CCAAT/ENHANCER-BINDING PROTEIN, EPSILON; CEBPE *600750 : PENTRAXIN II, NEURONAL; NPTX2 *600751 : SIALOADHESIN; SN *600752 : G PROTEIN-COUPLED RECEPTOR 12; GPR12 *600753 : GOLGI APPARATUS PROTEIN 1; GLG1 *600754 : MATRIX METALLOPROTEINASE 14; MMP14 *600755 : SYNAPSIN II; SYN2 *600756 : PROTEIN PHOSPHATASE 2A, REGULATORY SUBUNIT B-PRIME; PPP2R4 *600757 : OROFACIAL CLEFT 3; OFC3 *600758 : PROTEIN-TYROSINE KINASE, CYTOPLASMIC; PTK2 *600759 : ALZHEIMER DISEASE, FAMILIAL, TYPE 4 *600760 : SODIUM CHANNEL, NONVOLTAGE-GATED 1, BETA SUBUNIT; SCNN1B *600761 : SODIUM CHANNEL, NONVOLTAGE-GATED 1, GAMMA SUBUNIT; SCNN1G *600762 : HUMAN PAPILLOMAVIRUS E5 CENTRAL SEQUENCE-LIKE 1; HPVC1 *600763 : TUMOR PROTEIN, TRANSLATIONALLY-CONTROLLED 1; TPT1 *600764 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I-LIKE SEQUENCE; HLALS ^600765 : MOVED TO 600137 ^600766 : MOVED TO 300104 *600767 : GDP-DISSOCIATION INHIBITOR 2; GDI2 *600768 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 9; PTPN9 *600769 : TRANSMEMBRANE 4 SUPERFAMILY, MEMBER 3; TM4SF3 *600770 : MUCIN 5, SUBTYPE B, TRACHEOBRONCHIAL; MUC5B *600771 : DWARFISM, FAMILIAL, WITH MUSCLE SPASMS *600772 : TAF11 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 28-KD; TAF11 *600773 : TAF12 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 20-KD; TAF12 *600774 : TAF13 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 18-KD; TAF13 600775 : LAMBDOID SYNOSTOSIS 600776 : ANOPHTHALMIA-PLUS SYNDROME *600777 : TRANSCRIPTION TERMINATION FACTOR, RNA POLYMERASE I; TTF1 *600778 : CYCLIN-DEPENDENT KINASE INHIBITOR 1B; CDKN1B *600779 : FORKHEAD BOX G1A; FOXG1A ^600780 : MOVED TO 241410 *600781 : PEPTIDE YY; PYY *600782 : SYNAPTOTAGMIN 5; SYT5 *600783 : HISTIDYL-tRNA SYNTHETASE-LIKE; HARSL *600784 : GRANZYME K; GZMK *600785 : VITAMIN D-DEPENDENT RICKETS, RECEPTOR-POSITIVE TYPE *600786 : TRANSCRIPTION ELONGATION FACTOR B, 3; TCEB3 *600787 : TRANSCRIPTION ELONGATION FACTOR B, 2; TCEB2 *600788 : TRANSCRIPTION ELONGATION FACTOR B, 1; TCEB1 *600789 : RIBOSOMAL PROTEIN L23-LIKE; RPL23L *600790 : CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL #600791 : DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 4; DFNB4 *600792 : DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 5; DFNB5 ^600793 : MOVED TO 300081 *600794 : SPINAL MUSCULAR ATROPHY, DISTAL, WITH UPPER LIMB PREDOMINANCE *600795 : DEMENTIA, FAMILIAL NONSPECIFIC *600796 : SPLICING FACTOR 3A, SUBUNIT 2; SF3A2 *600797 : INSULIN RECEPTOR SUBSTRATE 2; IRS2 *600798 : HERPESVIRUS ENTRY MEDIATOR B; HVEB *600799 : BONE MORPHOGENETIC PROTEIN RECEPTOR, TYPE II; BMPR2 *600800 : NGFIA-BINDING PROTEIN; NAB1 600801 : ISOPROTERENOL-MEDIATED VASODILATATION #600802 : SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T-NEGATIVE/B-POSITIVE TYPE 600803 : CHOLELITHIASIS *600804 : MELATONIN RECEPTOR 1B; MTNR1B *600805 : LAMININ, ALPHA-3; LAMA3 *600806 : CALPONIN 1; CNN1 *600807 : ASTHMA *600808 : ENURESIS, NOCTURNAL, 2; ENUR2 ^600809 : MOVED TO 132890 *600810 : PHOSPHOLIPASE C, BETA-4; PLCB4 *600811 : DNA DAMAGE-BINDING PROTEIN 2; DDB2 *600812 : SPLICING FACTOR, ARGININE/SERINE-RICH, 1; SFRS1 *600813 : SPLICING FACTOR, ARGININE/SERINE-RICH, 2; SFRS2 *600814 : MEIOTIC RECOMBINATION 11, S. CEREVISIAE, HOMOLOG OF, A; MRE11A *600815 : POLYMERASE, DNA, DELTA, SMALL SUBUNIT; POLD2 *600816 : HEAT-SHOCK 70-KD PROTEIN 8; HSPA8 *600817 : VISININ-LIKE 1; VSNL1 *600818 : TRANSGELIN; TAGLN *600819 : FRAGILE X MENTAL RETARDATION, AUTOSOMAL HOMOLOG 1; FXR1 *600820 : ARCHAIN 1; ARCN1 *600821 : ARGININE VASOPRESSIN RECEPTOR 1A; AVPR1A *600822 : TAF9 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 32-KD; TAF9 *600823 : PROTEASE, SERINE, 8; PRSS8 *600824 : CYSTEINE- AND GLYCINE-RICH PROTEIN 3; CSRP3 *600825 : RAR-RELATED ORPHAN RECEPTOR A; RORA *600826 : CHONDROITIN SULFATE PROTEOGLYCAN 3; CSPG3 *600827 : PHOSPHODIESTERASE 6C, cGMP-SPECIFIC, CONE, ALPHA PRIME; PDE6C *600828 : ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL F1 COMPLEX, O SUBUNIT; ATP5O *600829 : INOSITOL POLYPHOSPHATE PHOSPHATASE-LIKE 1; INPPL1 *600830 : ZINC FINGER PROTEIN 173; ZNF173 *600831 : DEATH-ASSOCIATED PROTEIN KINASE 1; DAPK1 *600832 : ACIDIC LEUCINE-RICH NUCLEAR PHOSPHOPROTEIN 32 FAMILY, MEMBER A; ANP32A *600833 : SUPPRESSOR OF TUMORIGENICITY 7; ST7 *600834 : ZINC FINGER PROTEIN 165; ZNF165 *600835 : STROMAL CELL-DERIVED FACTOR 1; SDF1 *600836 : CRYSTALLIN, BETA-A2; CRYBA2 *600837 : GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR; GDNF *600838 : WINGED HELIX NUDE; WHN *600839 : SOLUTE CARRIER FAMILY 12 (SODIUM/POTASSIUM/CHLORIDE TRANSPORTER), MEMBER 1; SLC12A1 *600840 : SOLUTE CARRIER FAMILY 12 (SODIUM/POTASSIUM/CHLORIDE TRANSPORTER), MEMBER 2; SLC12A2 *600841 : EUKARYOTIC TRANSLATION ELONGATION FACTOR 1 ALPHA-1-LIKE 14; EEF1A1L14 *600842 : GLUCOKINASE REGULATORY PROTEIN; GCKR *600843 : PURINERGIC RECEPTOR P2X, LIGAND-GATED ION CHANNEL, 3; P2RX3 600844 : PURINERGIC RECEPTOR P2X, LIGAND-GATED ION CHANNEL, 2; P2RX2 *600845 : PURINERGIC RECEPTOR P2X, LIGAND-GATED ION CHANNEL, 1; P2RX1 *600846 : PURINERGIC RECEPTOR P2X, LIGAND-GATED ION CHANNEL, 4; P2RX4 ^600847 : MOVED TO 600695 *600848 : NUCLEAR RECEPTOR COREPRESSOR 2; NCOR2 *600849 : NUCLEAR RECEPTOR COREPRESSOR 1; NCOR1 *600850 : SCHIZOPHRENIA 4; SCZD4 600851 : MITOCHONDRIAL IMPORT-STIMULATING FACTOR *600852 : RETINITIS PIGMENTOSA 17; RP17 *600853 : N-DEACETYLASE/N-SULFOTRANSFERASE 1; NDST1 ^600854 : MOVED TO 600877 *600855 : DUAL-SPECIFICITY TYROSINE PHOSPHORYLATION-REGULATED KINASE 1A; DYRK1A *600856 : CYCLIN-DEPENDENT KINASE INHIBITOR 1C; CDKN1C *600857 : SUCCINATE DEHYDROGENASE COMPLEX, SUBUNIT A, FLAVOPROTEIN; SDHA #600858 : CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, WITH WOLFF-PARKINSON-WHITE SYNDROME *600859 : JTV1 GENE *600860 : GENERAL TRANSCRIPTION FACTOR IIIA; GTF3A *600861 : REGULATOR OF G PROTEIN SIGNALING 2; RGS2 *600862 : HIV-1 REV-BINDING PROTEIN; HRB *600863 : CASEIN KINASE I, EPSILON; CSNK1E *600864 : CASEIN KINASE I, DELTA; CSNK1D *600865 : RETICULON 1; RTN1 *600866 : PROGRAMMED CELL DEATH 2; PDCD2 *600867 : SIGNAL SEQUENCE RECEPTOR, BETA; SSR2 *600868 : SIGNAL SEQUENCE RECEPTOR, ALPHA; SSR1 *600869 : G PROTEIN-COUPLED RECEPTOR KINASE 6; GPRK6 *600870 : G PROTEIN-COUPLED RECEPTOR KINASE 5; GPRK5 *600871 : GROWTH FACTOR-INDEPENDENT 1; GFI1 ^600872 : MOVED TO 300113 *600873 : CHITOBIASE, DI-N-ACETYL- *600874 : GUANINE NUCLEOTIDE-BINDING PROTEIN, GAMMA-5; GNG5 *600875 : ACYLPHOSPHATASE, ERYTHROCYTE; ACYP1 *600876 : SYNTAXIN 3A; STX3A *600877 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 6; KCNJ6 600878 : RECEPTOR TYROSINE KINASE NSK2 *600879 : NUCLEAR RESPIRATORY FACTOR 1; NRF1 600880 : BUDD-CHIARI SYNDROME #600881 : CATARACT, CONGENITAL ZONULAR, WITH SUTURAL OPACITIES; CCZS *600882 : CHARCOT-MARIE-TOOTH DISEASE, NEURONAL TYPE, B; CMT2B *600883 : DIABETES MELLITUS, INSULIN-DEPENDENT, 8; IDDM8 *600884 : CARDIOMYOPATHY, DILATED, 1B; CMD1B #600885 : BERLIN BREAKAGE SYNDROME #600886 : HYPERFERRITINEMIA-CATARACT SYNDROME *600887 : MutS, E. COLI, HOMOLOG OF, 3; MSH3 *600888 : RHO GUANINE NUCLEOTIDE EXCHANGE FACTOR 5; ARHGEF5 *600889 : FACTOR H-RELATED GENE 2; FHR2 *600890 : HYDROXYACYL-CoA DEHYDROGENASE/3-KETOACYL-CoA THIOLASE/ENOYL-CoA HYDRATASE, ALPHA SUBUNIT; HADHA ^600891 : MOVED TO 300098 *600892 : SINGLE-MINDED, DROSOPHILA, HOMOLOG OF, 2; SIM2 ^600893 : MOVED TO 300099 *600894 : G PROTEIN-COUPLED RECEPTOR 9; GPR9 *600895 : G PROTEIN-COUPLED RECEPTOR 10; GPR10 600896 : G PROTEIN-COUPLED RECEPTOR 14; GPR14 *600897 : GAP JUNCTION PROTEIN, ALPHA-8; GJA8 *600898 : SRY-BOX 11; SOX11 *600899 : PROTEIN KINASE, DNA-ACTIVATED, CATALYTIC SUBUNIT; PRKDC *600900 : SARCOGLYCAN, BETA; SGCB *600901 : FANCONI ANEMIA, COMPLEMENTATION GROUP E; FANCE *600902 : SELENOPHOSPHATE SYNTHETASE 600903 : WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM *600904 : ASTROTACTIN; ASTN ^600905 : MOVED TO 600600 600906 : ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY 600907 : ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS 600908 : AGONADISM, XY, WITH MENTAL RETARDATION, SHORT STATURE, RETARDED BONE AGE, AND MULTIPLE EXTRAGENITAL MALFORMATIONS *600909 : LANOSTEROL SYNTHASE; LSS *600910 : INSULIN-LIKE 4; INSL4 *600911 : CHROMOSOME 11 OPEN READING FRAME 8; C11ORF8 *600912 : TRANSCRIPTION FACTOR 19; TCF19 600913 : DELAYED-EARLY INSULIN-INDUCED GENE CL-6 *600914 : SPLICING FACTOR, ARGININE/SERINE-RICH, 5; SFRS5 *600915 : NESTIN; NES *600916 : INOSITOL POLYPHOSPHATE-4-PHOSPHATASE, TYPE I, 107-KD; INPP4A *600917 : PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 3A; PPP1R3A #600918 : CYSTINURIA, TYPE III; CSNU3 *600919 : LONG QT SYNDROME 4; LQT4 600920 : MARDEN-WALKER-LIKE SYNDROME WITHOUT PSYCHOMOTOR RETARDATION *600921 : FIBROBLAST GROWTH FACTOR 9; FGF9 *600922 : MYOSIN LIGHT CHAIN KINASE; MYLK *600923 : PROTOPORPHYRINOGEN OXIDASE; PPOX *600924 : GROWTH FACTOR, ERV1-LIKE; GFER *600925 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, J; PTPRJ *600926 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, EPSILON; PTPRE *600927 : CYCLIN-DEPENDENT KINASE INHIBITOR 2D; CDKN2D *600928 : CONSERVED GENE TELOMERIC TO ALPHA GLOBIN CLUSTER *600929 : CRYSTALLIN, BETA-B1; CRYBB1 *600930 : SPERM ADHESION MOLECULE 1; SPAM1 600931 : PROTOCADHERIN 3 *600932 : G PROTEIN-COUPLED INWARD RECTIFIER POTASSIUM CHANNEL *600933 : COAGULATION FACTOR II RECEPTOR-LIKE 1; F2RL1 *600934 : FOLATE HYDROLASE 1; FOLH1 *600935 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 8; KCNJ8 *600936 : HYALURONAN-MEDIATED MOTILITY RECEPTOR; HMMR *600937 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 11; KCNJ11 *600938 : RETINOBLASTOMA-BINDING PROTEIN 6; RBBP6 *600939 : INTERLEUKIN 11 RECEPTOR, ALPHA; IL11RA *600940 : LIGASE III, DNA, ATP-DEPENDENT; LIG3 *600941 : BILIVERDIN REDUCTASE B; BLVRB *600942 : COLLAGEN-BINDING PROTEIN 1; CBP1 *600943 : COLLAGEN-BINDING PROTEIN 2; CBP2 *600944 : DEOXYHYPUSINE SYNTHASE; DHPS *600945 : UROCORTIN; UCN *600946 : GROWTH HORMONE RECEPTOR; GHR *600947 : HUNTINGTIN-ASSOCIATED PROTEIN 1; HAP1 *600948 : MYELIN-ASSOCIATED OLIGODENDROCYTE BASIC PROTEIN; MOBP *600949 : IMMUNOGLOBULIN HEAVY CHAIN VARIABLE REGION-2 *600950 : ARYLALKYLAMINE N-ACETYLTRANSFERASE; AANAT *600951 : TELOMERIC REPEAT-BINDING FACTOR 1; TERF1 600952 : TRANSSEXUALITY *600953 : INTERLEUKIN 18; IL18 *600954 : DEATH-ASSOCIATED PROTEIN; DAP #600955 : OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES *600956 : ANTI-MULLERIAN HORMONE TYPE II RECEPTOR; AMHR2 *600957 : ANTI-MULLERIAN HORMONE; AMH *600958 : MYOSIN-BINDING PROTEIN C, CARDIAC; MYBPC3 *600959 : COATOMER PROTEIN COMPLEX, SUBUNIT BETA; COPB *600960 : SET TRANSLOCATION, MYELOID LEUKEMIA-ASSOCIATED; SET ^600961 : MOVED TO 601498 #600962 : NONEPIDERMOLYTIC PALMOPLANTAR KERATODERMA; NEPPK *600963 : SINE OCULIS HOMEO BOX, DROSOPHILA, HOMOLOG OF, 5; SIX5 *600964 : REFSUM DISEASE WITH INCREASED PIPECOLICACIDEMIA; RDPA #600965 : HEARING LOSS, LOW-FREQUENCY SENSORINEURAL; LFSNHL *600966 : LETHAL GIANT LARVAE, DROSOPHILA, HOMOLOG OF, 1; LLGL1 *600967 : E2F TRANSCRIPTION FACTOR 5; E2F5 *600968 : SOLUTE CARRIER FAMILY 12 (SODIUM/CHLORIDE TRANSPORTER), MEMBER 3; SLC12A3 #600969 : EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3 *600970 : MYOSIN VI; MYO6 *600971 : DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 6; DFNB6 #600972 : ACHONDROGENESIS, TYPE IB; ACG1B ^600973 : MOVED TO 600308 #600974 : DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 7; DFNB7 *600975 : GLAUCOMA 3, PRIMARY INFANTILE, B; GLC3B *600976 : FAT TUMOR SUPPRESSOR, DROSOPHILA, HOMOLOG OF; FAT *600977 : CONE-ROD DYSTROPHY 5; CORD5 *600978 : LYMPHOTOXIN-BETA; LTB *600979 : LYMPHOTOXIN B RECEPTOR; LTBR *600980 : DENTIN MATRIX ACIDIC PHOSPHOPROTEIN 1; DMP1 *600981 : PHOSPHOGLUCOMUTASE 5; PGM5 *600982 : MITOGEN-ACTIVATED KINASE KINASE KINASE 1; MAP3K1 *600983 : NUCLEAR RECEPTOR SUBFAMILY 3, GROUP C, MEMBER 2; NR3C2 *600984 : cAMP RESPONSE ELEMENT-BINDING PROTEIN-LIKE 1; CREBL1 *600985 : TENASCIN-XB; TNXB *600986 : GENE Y; GENEY 600987 : CARDIAC MALFORMATION, CLEFT LIP-PALATE, MICROCEPHALY AND DIGITAL ANOMALIES *600988 : MANNOSIDASE, ALPHA, CLASS 2A, MEMBER 2; MAN2A2 600989 : INFUNDIBULOPELVIC DYSGENESIS *600990 : LAGOPHTHALMIA WITH BILATERAL CLEFT LIP AND PALATE 600991 : HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE 600992 : ANOPHTHALMIA AND ESOPHAGEAL ATRESIA *600993 : MOTHERS AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 4; MADH4 *600994 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 5; DFNA5 #600995 : NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1 #600996 : ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2; ARVD2 *600997 : EPHRIN RECEPTOR EphB2; EPHB2 *600998 : GUANINE NUCLEOTIDE-BINDING PROTEIN, Q POLYPEPTIDE; GNAQ *600999 : MYC-ASSOCIATED ZINC FINGER PROTEIN; MAZ ^601000 : MOVED TO 109170 #601001 : EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE *601002 : GLUTATHIONE SYNTHETASE; GSS #601003 : BRODY MYOPATHY 601004 : PORTAL VEIN, CAVERNOUS TRANSFORMATION OF 601005 : LONG QT SYNDROME WITH SYNDACTYLY ^601006 : MOVED TO 138890 *601007 : LEPTIN RECEPTOR; LEPR ^601008 : MOVED TO 148760 *601009 : TIGHT JUNCTION PROTEIN 1; TJP1 *601010 : TRANSCRIPTION FACTOR 15; TCF15 *601011 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, P/Q TYPE, ALPHA-1A SUBUNIT; CACNA1A *601012 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, N TYPE, ALPHA-1B SUBUNIT; CACNA1B *601013 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, ALPHA-1E SUBUNIT; CACNA1E *601014 : DISCS LARGE, DROSOPHILA, HOMOLOG OF, 1; DLG1 *601015 : NIEMANN-PICK DISEASE, TYPE C2 GENE; NPC2 601016 : MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM *601017 : SYNTROPHIN, ALPHA-1; SNTA1 ^601018 : MOVED TO 600027 *601019 : SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, GLYCINE), MEMBER 9; SLC6A9 *601020 : CD86 ANTIGEN; CD86 *601021 : NUCLEOPORIN, 98-KD; NUP98 *601022 : NUCLEAR FACTOR OF KAPPA LIGHT CHAIN GENE ENHANCER IN B CELLS INHIBITOR-LIKE 1; NFKBIL1 *601023 : VALOSIN-CONTAINING PROTEIN; VCP *601024 : ADAPTOR-RELATED PROTEIN COMPLEX 2, MU-1 SUBUNIT; AP2M1 *601025 : ADAPTOR-RELATED PROTEIN COMPLEX 2, BETA-1 SUBUNIT; AP2B1 601026 : ADAPTOR-RELATED PROTEIN COMPLEX 2, ALPHA-1 SUBUNIT; AP2A1 601027 : TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES *601028 : CD47 ANTIGEN; CD47 *601029 : MESODERM-SPECIFIC TRANSCRIPT, MOUSE, HOMOLOG OF; MEST *601030 : RIBONUCLEASE A FAMILY, 4; RNASE4 601031 : RHOPHILIN *601032 : PROTEIN KINASE C-LIKE 1; PRKCL1 *601033 : LAMININ, ALPHA-5; LAMA5 601034 : GICERIN *601035 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H1; HNRPH1 *601036 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H2; HNRPH2 *601037 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN F; HNRPF *601038 : DEIODINASE, IODOTHYRONINE, TYPE III; DIO3 601039 : ICHTHYOSIS-MENTAL RETARDATION SYNDROME WITH LARGE KERATOHYALIN GRANULES IN THE SKIN *601040 : CD36 ANTIGEN-LIKE 1; CD36L1 *601041 : TRANSDUCIN-LIKE ENHANCER OF SPLIT 2; TLE2 *601042 : CHOREOATHETOSIS/SPASTICITY, EPISODIC; CSE *601043 : INSULIN RECEPTOR GENE TRANSCRIPTION FACTOR 1; IRTF1 *601044 : INSULIN RECEPTOR GENE TRANSCRIPTION FACTOR 2; IRTF2 *601045 : CATENIN, DELTA-1; CTNND1 *601046 : MATRIX METALLOPROTEINASE 12; MMP12 *601047 : CAVEOLIN 1; CAV1 *601048 : CAVEOLIN 2; CAV2 ^601049 : MOVED TO 300119 ^601050 : REMOVED FROM DATABASE *601051 : MESOTHELIN; MSLN *601052 : PEPTIDYL-PROLYL CIS/TRANS ISOMERASE, NIMA-INTERACTING, 1; PIN1 *601053 : PLEXIN B1; PLXNB1 *601054 : PLEXIN A2; PLXNA2 *601055 : PLEXIN A1; PLXNA1 *601056 : BCL2-RELATED PROTEIN A1; BCL2A1 *601057 : PROGRAMMED CELL DEATH 6; PDCD6 *601058 : H3 HISTONE, FAMILY 3B; H3F3B *601059 : ADENOSINE DEAMINASE, RNA-SPECIFIC; ADAR *601060 : ECTONUCLEOTIDE PYROPHOSPHATASE/PHOSPHODIESTERASE 2; ENPP2 *601061 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE D2; SNRPD2 *601062 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE D3; SNRPD3 *601063 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE D1; SNRPD1 *601064 : ZINC FINGER PROTEIN 36, C3H TYPE-LIKE 1; ZFP36L1 *601065 : ALANYL-tRNA SYNTHETASE; AARS *601066 : OXIDASE, CYTOCHROME c, ASSEMBLY 1-LIKE; OXA1L #601067 : USHER SYNDROME, TYPE ID; USH1D *601068 : EPILEPSY, MYOCLONIC, BENIGN ADULT FAMILIAL *601069 : ZINC FINGER PROTEIN 239; ZNF239 *601070 : INTERLEUKIN 15 RECEPTOR, ALPHA; IL15RA #601071 : DEAFNESS, AUTOSOMAL RECESSIVE 9; DFNB9 #601072 : DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8; DFNB8 ^601073 : MOVED TO 600737 *601074 : CUG TRIPLET REPEAT, RNA-BINDING PROTEIN 1; CUGBP1 601075 : APLASIA CUTIS CONGENITA, HIGH MYOPIA, AND CONE-ROD DYSFUNCTION ^601076 : MOVED TO 223340 *601077 : KERATIN, HAIR, ACIDIC, 1; KRTHA1 *601078 : KERATIN, HAIR, BASIC, 2; KRTHB2 *601079 : U2 SMALL NUCLEAR RIBONUCLEOPROTEIN AUXILIARY FACTOR, SMALL SUBUNIT 1 *601080 : U2 SMALL NUCLEAR RIBONUCLEOPROTEIN AUXILIARY FACTOR, SMALL SUBUNIT 3; U2AF1RS3 *601081 : ATP-BINDING CASSETTE, SUBFAMILY 3, MEMBER 2; ABCD2 *601082 : UBIQUITIN-CONJUGATING ENZYME E2H; UBE2H 601083 : CD4/CD8 T-CELL RATIO *601084 : CANCER CACHECTIC FACTOR 1 601085 : ROLANDIC EPILEPSY AND SPEECH DYSPRAXIA *601086 : LATERALITY DEFECTS, AUTOSOMAL DOMINANT ^601087 : MOVED TO 121210 601088 : CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKE FACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION *601089 : FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 5; FKHL5 *601090 : FORKHEAD BOX CI; FOXC1 *601091 : FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 8; FKHL8 *601092 : FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 9; FKHL9 *601093 : FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 10; FKHL10 *601094 : FORKHEAD BOX E3; FOXE3 601095 : HARROD SYNDROME 601096 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MICROMELIC *601097 : PERIPHERAL MYELIN PROTEIN 22; PMP22 *601098 : CHARCOT-MARIE-TOOTH DISEASE, TYPE 1C; CMT1C *601099 : SRC-LIKE ADAPTOR; SLA *601100 : STRESS 70 PROTEIN CHAPERONE, MICROSOME-ASSOCIATED, 60-KD; STCH 601101 : OSLER-RENDU-WEBER SYNDROME 3; ORW3 *601102 : EUKARYOTIC TRANSLATION INITIATION FACTOR 4A, ISOFORM 2; EIF4A2 *601103 : MICROFIBRIL-ASSOCIATED GLYCOPROTEIN 2 *601104 : SUPRANUCLEAR PALSY, PROGRESSIVE; PSP *601105 : CATHEPSIN K; CTSK *601106 : BB1 GENE *601107 : ATP-BINDING CASSETTE, SUBFAMILY C, MEMBER 2; ABCC2 ^601108 : MOVED TO 300283 *601109 : 5-@HYDROXYTRYPTAMINE RECEPTOR 6; HTR6 *601110 : CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id ^601111 : MOVED TO 600941 *601112 : THIOREDOXIN REDUCTASE 1; TXNRD1 *601113 : HEAT-SHOCK 70-KD PROTEIN 4; HSPA4 *601114 : MEMBRANE PROTEIN, PALMITOYLATED 3; MPP3 *601115 : GLUTAMATE RECEPTOR, METABOTROPIC, 3; GRM3 *601116 : GLUTAMATE RECEPTOR, METABOTROPIC, 8; GRM8 *601117 : THIMET OLIGOPEPTIDASE 1; THOP1 *601118 : CALCIUM-MODULATING CYCLOPHILIN LIGAND; CAMLG *601119 : CLpP, E. COLI, HOMOLOG OF; CLPP *601120 : CADHERIN 5; CDH5 *601121 : PLACENTAL GROWTH FACTOR; PGF *601122 : 5-@HYDROXYTRYPTAMINE RECEPTOR 2B; HTR2B *601123 : SIALYLTRANSFERASE 8; SIAT8 *601124 : SEMAPHORIN 3F; SEMA3F *601125 : HEXOKINASE 2; HK2 *601126 : TATA ELEMENT MODULATORY FACTOR 1; TMF1 601127 : FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION *601128 : H3 HISTONE, FAMILY 3A; H3F3A *601129 : CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 8; CYP2C8 *601130 : CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 9; CYP2C9 *601131 : CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 18; CYP2C18 *601132 : KINASE SUPPRESSOR OF RAS; KSR *601133 : CYTOCHROME P450, SUBFAMILY IIG, POLYPEPTIDE 1; CYP2G1 *601134 : INTEGRAL MEMBRANE PROTEIN 1; ITM1 *601135 : GASTRULATION BRAIN HOMEO BOX 2; GBX2 *601136 : TRANSSUPPRESSOR OF EXPRESSION 2; TSE2 601137 : GUANYLYL CYCLASE, MEMBRANE, TYPE D, MURINE 601138 : GUANYLYL CYCLASE, MEMBRANE, TYPE E; GUCY2E *601139 : ZINC FINGER PROTEIN 175; ZNF175 *601140 : PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 14B; PPP1R14B *601141 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAKER-RELATED SUBFAMILY, BETA MEMBER 1; KCNAB1 *601142 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAKER-RELATED SUBFAMILY, BETA MEMBER 2; KCNAB2 *601143 : DYNACTIN 1; DCTN1 #601144 : BRUGADA SYNDROME *601145 : CYSTATIN B; CSTB *601146 : GROWTH/DIFFERENTIATION FACTOR 5; GDF5 *601147 : CARTILAGE-DERIVED MORPHOGENETIC PROTEIN 2 *601148 : MITOCHONDRIAL CAPSULE SELENOPROTEIN; MCSP *601149 : ISOCITRATE DEHYDROGENASE 3, ALPHA SUBUNIT; IDH3A *601150 : DEAD/H BOX 11; DDX11 *601151 : DEAD/H BOX 12; DDX12 601152 : PERIPHERAL NEUROPATHY AND OPTIC ATROPHY *601153 : FRAGILE HISTIDINE TRIAD GENE; FHIT *601154 : CARDIOMYOPATHY, DILATED, 1E; CMD1E *601155 : MINOR HISTOCOMPATIBILITY ANTIGEN HA-1 *601156 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 11; SCYA11 *601157 : DEFENSIN, ALPHA, 4; DEFA4 *601158 : MITOGEN-ACTIVATED PROTEIN KINASE 8; MAPK8 *601159 : CHEMOKINE (C-C) RECEPTOR 1; CCR1 601160 : LISSENCEPHALY TYPE III AND BONE DYSPLASIA 601161 : TRISOMY 18-LIKE SYNDROME *601162 : SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT; SPG9 601163 : DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL 601164 : EXTRAPYRAMIDAL DISORDER, PROGRESSIVE, WITH PRIMARY HYPOGONADISM AND ALOPECIA 601165 : CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION, AND LETHAL CONGENITAL HEART DISEASE *601166 : G PROTEIN-COUPLED RECEPTOR 15; GPR15 *601167 : PURINERGIC RECEPTOR P2Y, G PROTEIN-COUPLED, 1; P2RY1 *601168 : DIHYDROPYRIMIDINASE-LIKE 3; DPYSL3 ^601169 : REMOVED FROM DATABASE 601170 : MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS 601171 : SERPIN-LIKE PROTEIN B43, BOVINE *601172 : CHONDROITIN SULFATE PROTEOGLYCAN 4; CSPG4 #601173 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 601174 : IMIDAZOLINE RECEPTOR *601175 : ADP-RIBOSYLATION FACTOR-LIKE 2; ARL2 *601176 : GLUTAMATE-CYSTEINE LIGASE, MODIFIER SUBUNIT; GCLM *601177 : ADP-RIBOSYLATION FACTOR 4; ARF4 *601178 : MEMBRANE COMPONENT, CHROMOSOME 11, SURFACE MARKER 1; M11S1 *601179 : RAS-RELATED NUCLEAR PROTEIN; RAN *601180 : RAN-BINDING PROTEIN 1; RANBP1 *601181 : RAN-BINDING PROTEIN 2; RANBP2 *601182 : ORIGIN RECOGNITION COMPLEX, SUBUNIT 2, S. CEREVISIAE, HOMOLOG OF; ORC2L *601183 : CYSTEINE-RICH INTESTINAL PROTEIN 2; CRIP2 *601184 : DNAJ, E. COLI, HOMOLOG OF, SUBFAMILY C, MEMBER 3; DNAJC3 *601185 : STANNIOCALCIN 1; STC1 601186 : ANOPHTHALMIA AND PULMONARY HYPOPLASIA 601187 : GURRIERI SYNDROME *601188 : SUPPRESSION OF TUMORIGENICITY 12; ST12 *601189 : POLYMERASE II, RNA, SUBUNIT L; POLR2L *601190 : PHOSPHODIESTERASE 6H, cGMP-SPECIFIC, CONE, GAMMA; PDE6H *601191 : ENHANCER OF RUDIMENTARY, DROSOPHILA, HOMOLOG OF; ERH *601192 : PHOSPHOLIPASE A2, GROUP V; PLA2G5 *601193 : ACIDIC EPIDIDYMAL GLYCOPROTEIN-LIKE 1; AEGL1 *601194 : TOLL-LIKE RECEPTOR 1; TLR1 601195 : IRON OVERLOAD IN AFRICA *601196 : PR DOMAIN-CONTAINING PROTEIN 2; PRDM2 *601197 : TUBBY, MOUSE, HOMOLOG OF; TUB #601198 : HYPOCALCEMIA, AUTOSOMAL DOMINANT *601199 : CALCIUM-SENSING RECEPTOR; CASR 601200 : PLEUROPULMONARY BLASTOMA *601201 : METHYLATION MODIFIER FOR CLASS I HLA *601202 : CATARACT, ANTERIOR POLAR, 2; CTAA2 *601203 : INTERLEUKIN 1 RECEPTOR-LIKE 1; IL1RL1 *601204 : PROSTAGLANDIN F2 RECEPTOR NEGATIVE REGULATOR; PTGFRN *601205 : SINE OCULIS HOMEO BOX, DROSOPHILA, HOMOLOG OF, 1; SIX1 *601206 : POU DOMAIN, CLASS 2, ASSOCIATING FACTOR 1; POU2AF1 *601207 : DIACYLGLYCEROL KINASE, THETA, 110-KD; DGKQ *601208 : DIABETES MELLITUS, INSULIN-DEPENDENT, 11; IDDM11 *601209 : POLY(rC)-BINDING PROTEIN 1; PCBP1 *601210 : POLY(rC)-BINDING PROTEIN 2; PCBP2 *601211 : CD97 ANTIGEN; CD97 *601212 : PROTEIN-TYROSINE KINASE 2, BETA; PTK2B *601213 : RIBONUCLEASE 4 INHIBITOR; RNS4I #601214 : NAXOS DISEASE *601215 : ATAXIA-TELANGIECTASIA AND RAD3-RELATED; ATR 601216 : PLATYSPONDYLY WITH AMELOGENESIS IMPERFECTA 601217 : ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPIC HYPOGONADISM *601218 : ADENOSINE DEAMINASE, RNA-SPECIFIC, B1; ADARB1 *601219 : SODIUM CHANNEL, VOLTAGE-GATED, TYPE II, ALPHA-2 SUBUNIT; SCN2A2 601220 : OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME; OOCH *601221 : TISSUE SPECIFIC EXTINGUISHER 3 601222 : CRANIOSYNOSTOSIS, PHILADELPHIA TYPE 601223 : NEURONAL INTESTINAL DYSPLASIA, TYPE B; NID B #601224 : POTOCKI-SHAFFER SYNDROME *601225 : DISHEVELLED 1-LIKE 1; DVL1L1 ^601226 : MOVED TO 601227 ^601227 : MOVED TO 157640 *601228 : POLYPOSIS SYNDROME, MIXED, HEREDITARY ^601229 : MOVED TO 151430 601230 : DERMATITIS HERPETIFORMIS, FAMILIAL *601231 : FKBP12-RAPAMYCIN COMPLEX-ASSOCIATED PROTEIN 1; FRAP1 *601232 : PHOSPHATIDYLINOSITOL 3-KINASE, CATALYTIC, GAMMA; PIK3CG *601233 : INHIBIN, BETA C; INHBC *601234 : NASCENT-POLYPEPTIDE-ASSOCIATED COMPLEX, ALPHA POLYPEPTIDE; NACA *601235 : DEAD/H BOX 10; DDX10 *601236 : DISABLED, DROSOPHILA, HOMOLOG OF, 2; DAB2 *601237 : ZINC FINGER PROTEIN 179; ZNF179 *601238 : CEREBELLAR ATAXIA, CAYMAN TYPE; ATCAY *601239 : DYSTROBREVIN, ALPHA; DTNA *601240 : GUANIDINOACETATE METHYLTRANSFERASE; GAMT *601241 : HISTONE DEACETYLASE 1; HDAC1 *601242 : MICROTUBULE-ASSOCIATED PROTEINS 1A AND 1B, LIGHT CHAIN 3 *601243 : TOPOISOMERASE, DNA, III, ALPHA; TOP3A *601244 : GUANYLATE CYCLASE 1, SOLUBLE, ALPHA-2; GUCY1A2 *601245 : CHROMATIN ASSEMBLY FACTOR I, SUBUNIT B; CHAF1B *601246 : CHROMATIN ASSEMBLY FACTOR I, SUBUNIT A; CHAF1A *601247 : SON OF SEVENLESS, DROSOPHILA, HOMOLOG 2; SOS2 *601248 : BRIDGING INTEGRATOR 1; BIN1 *601249 : PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE-ASSOCIATED PROTEIN 1; PRPSAP1 *601250 : PEPTIDE METHIONINE SULFOXIDE REDUCTASE; MSRA *601251 : RETINAL CONE DYSTROPHY 2 *601252 : FICOLIN 1; FCN1 *601253 : CAVEOLIN 3; CAV3 *601254 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE 6; MAP2K6 *601255 : AXONAL TRANSPORTER OF SYNAPTIC VESICLES; ATSV *601256 : ANGIOTENSIN RECEPTOR-LIKE 2; AGTRL2 *601257 : DEAD/H BOX 1; DDX1 *601258 : CYTOCHROME P450, SUBFAMILY IIJ, POLYPEPTIDE 2; CYP2J2 *601259 : AMELOBLASTIN ENAMEL MATRIX PROTEIN; AMBN *601260 : ZINC FINGER PROTEIN 36; ZNF36 *601261 : ZINC FINGER PROTEIN 38; ZNF38 *601262 : ZINC FINGER PROTEIN 16; ZNF16 *601263 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE 2; MAP2K2 *601264 : GUANYLATE CYCLASE C ACTIVATING PEPTIDE II *601265 : NODAL, MOUSE, HOMOLOG OF; NODAL *601266 : dUTP PYROPHOSPHATASE; DUT *601267 : CHEMOKINE (C-C) RECEPTOR 2; CCR2 *601268 : CHEMOKINE (C-C) RECEPTOR 3; CCR3 *601269 : COMPLEMENT COMPONENT C1q-BINDING PROTEIN; C1QBP *601270 : CYTOCHROME P450, SUBFAMILY IVF, POLYPEPTIDE 3; CYP4F3 *601271 : GUANYLATE CYCLASE ACTIVATOR 2B; GUCA2B *601272 : SORTING NEXIN 1; SNX1 *601273 : CLATHRIN, HEAVY POLYPEPTIDE-LIKE 1; CLTCL1 601274 : LEUKOTRIENE B4 12-HYDROXYDEHYDROGENASE *601275 : GLYCOPROTEIN M6A; GPM6A 601276 : ZINC FINGER GENE 177; ZNF177 *601277 : ICHTHYOSIS, LAMELLAR, 2; LI2 *601278 : FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY REGION GENE 1; FRG1 *601279 : DIGEORGE SYNDROME CRITICAL REGION 6; DGCR6 *601280 : MAB21, C. ELEGANS, HOMOLOG-LIKE 1; MAB21L1 *601281 : SEMAPHORIN 3B; SEMA3B *601282 : PLECTIN 1; PLEC1 *601283 : DIABETES MELLITUS, NONINSULIN-DEPENDENT, 1; NIDDM1 *601284 : ACTIVIN A RECEPTOR, TYPE II-LIKE KINASE 1; ACVRL1 *601285 : DELETED IN SPLIT-HAND/SPLIT-FOOT 1 REGION *601286 : CATARACT, NONNUCLEAR POLYMORPHIC CONGENITAL, AUTOSOMAL DOMINANT #601287 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F; LGMD2F *601288 : TYROSINE 3-MONOOXYGENASE/TRYPTOPHAN 5-MONOOXYGENASE ACTIVATION PROTEIN, ZETA ISOFORM; YWHAZ *601289 : TYROSINE 3-MONOOXYGENASE/TRYPTOPHAN 5-MONOOXYGENASE ACTIVATION PROTEIN, BETA ISOFORM; YWHAB *601290 : STRATIFIN; SFN *601291 : URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASE 8; UGT8 *601292 : SULFOTRANSFERASE FAMILY 1A, PHENOL-PREFERRING, MEMBER 2; SULT1A2 *601293 : RAS HOMOLOG ENRICHED IN BRAIN 2; RHEB2 *601294 : SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, CREATINE), MEMBER 10; SLC6A10 *601295 : SOLUTE CARRIER FAMILY 10 (SODIUM/BILE ACID COTRANSPORTER FAMILY), MEMBER 2; SLC10A2 *601296 : MUSCLE, SKELETAL, RECEPTOR TYROSINE KINASE; MUSK *601297 : SRY-BOX 20; SOX20 ^601298 : MOVED TO 102576 *601299 : BONE MORPHOGENETIC PROTEIN RECEPTOR, TYPE IA; BMPR1A *601300 : ACTIVIN A RECEPTOR, TYPE IB; ACVR1B *601301 : PEPTIDYL-PROLYL ISOMERASE-LIKE 1; PPIL1 *601302 : PROTEIN PHOSPHATASE 3, REGULATORY SUBUNIT B, ALPHA ISOFORM 1; PPP3R1 *601303 : CYTOSKELETON-ASSOCIATED PROTEIN 1; CKAP1 *601304 : NON-HISTONE CHROMOSOME PROTEIN 2, S. CEREVISIAE, HOMOLOG-LIKE 1; NHP2L1 *601305 : 5-@HYDROXYTRYPTAMINE RECEPTOR 5A; HTR5A *601306 : HEMATOPOIETIC CELL-SPECIFIC LYN SUBSTRATE 1; HCLS1 ^601307 : MOVED TO 600924 *601308 : MYELOID LEUKEMIA-RELATED GENE *601309 : PATCHED, DROSOPHILA, HOMOLOG OF; PTCH *601310 : CYTOCHROME P450, SUBFAMILY IVA, POLYPEPTIDE 11; CYP4A11 *601311 : STEROL O-ACYLTRANSFERASE 2; SOAT2 ^601312 : MOVED TO 600408 *601313 : POLYCYSTIC KIDNEY DISEASE 1; PKD1 *601314 : HISTIDINE TRIAD NUCLEOTIDE-BINDING PROTEIN; HINT 601315 : EPITHELIAL BASOLATERAL CHLORIDE CONDUCTANCE REGULATOR, RABBIT, HOMOLOG OF #601316 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 10; DFNA10 *601317 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 11; DFNA11 *601318 : DIABETES MELLITUS, INSULIN-DEPENDENT, 13; IDDM13 601319 : ODONTOMICRONYCHIAL DYSPLASIA ^601320 : MOVED TO 601984 601321 : NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS 601322 : PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS *601323 : NUCLEOBINDIN 1; NUCB1 *601324 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN D; HNRPD *601325 : CONTACTIN 3; CNTN3 *601326 : CLAUDIN 11; CLDN11 *601327 : SODIUM CHANNEL, VOLTAGE-GATED, TYPE II, BETA SUBUNIT; SCN2B *601328 : SODIUM CHANNEL, NONVOLTAGE-GATED 1, DELTA SUBUNIT; SCNN1D *601329 : LIM DOMAIN KINASE 1; LIMK1 *601330 : GUANYLATE CYCLASE 2C; GUCY2C 601331 : RENAL DYSPLASIA, DIFFUSE CYSTIC *601332 : TWIRLER MUTATION, MURINE, HUMAN HOMOLOG OF *601333 : SUPPRESSOR OF TY 6, S. CEREVISIAE, HOMOLOG OF; SUPT6H *601334 : KINESIN, LIGHT CHAIN, 2 *601335 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE 4; MAP2K4 *601336 : GLUCOSIDASE I; GCS1 *601337 : REGULATORY FACTOR X, 3; RFX3 601338 : CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS *601339 : THIOREDOXIN REDUCTASE, SELENOCYSTEINE-CONTAINING *601340 : MELANOMA-INHIBITORY ACTIVITY; MIA 601341 : ATROPHIA MACULOSA VARIOLIFORMIS CUTIS, FAMILIAL; AMVC *601342 : CHROMOSOME SEGREGATION 1-LIKE; CSE1L ^601343 : MOVED TO 276821 601344 : SPINAL DYSPLASIA, ANHALT TYPE 601345 : ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE 601346 : GASTROINTESTINAL ABNORMALITIES, MULTIPLE 601347 : MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE, AND PSYCHOMOTOR DELAY 601348 : ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA 601349 : MICROCEPHALY, MICROPHTHALMIA, ECTRODACTYLY OF LOWER LIMBS, AND PROGNATHISM; MMEP 601350 : SHORT STATURE SYNDROME, BRUSSELS TYPE 601351 : GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION 601352 : MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE 601353 : BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION ^601354 : MOVED TO 300166 601355 : MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS, AND HYPOSEGMENTED LUNGS 601356 : LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE 601357 : BRACHIAL AMELIA, FOREBRAIN DEFECTS, AND FACIAL CLEFTS 601358 : SPARSE HAIR AND MENTAL RETARDATION 601359 : SEBACEOUS NEVUS SYNDROME AND HEMIMEGALENCEPHALY 601360 : AMELIA, AUTOSOMAL RECESSIVE *601361 : GROWTH/DIFFERENTIATION FACTOR 10; GDF10 *601362 : DIGEORGE SYNDROME/VELOCARDIOFACIAL SYNDROME SPECTRUM OF MALFORMATION 2 *601363 : WILMS TUMOR 4 *601364 : CADHERIN 13; CDH13 *601365 : DISHEVELLED 1; DVL1 *601366 : MOTHERS AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 2; MADH2 *601367 : STROKE *601368 : DISHEVELLED 3; DVL3 #601369 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 9; DFNA9 601370 : HOLOPROSENCEPHALY, SEMILOBAR, WITH CRANIOSYNOSTOSIS 601371 : NUCLEAR SCLEROSIS OF THE LENS 601372 : CHOREA, REMITTING, WITH NYSTAGMUS AND CATARACT *601373 : CHEMOKINE (C-C) RECEPTOR 5; CCR5 601374 : APROSENCEPHALY AND CEREBELLAR DYSGENESIS 601375 : ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE 601376 : CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY ^601377 : MOVED TO 218340 601378 : CRISPONI SYNDROME 601379 : HUNTER-MCALPINE CRANIOSYNOSTOSIS SYNDROME *601380 : EPHRIN A4; EFNA4 *601381 : EPHRIN A3; EFNA3 #601382 : CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B; CMT4B *601383 : AQUAPORIN 6; AQP6 *601384 : LYMPHOCYTE ANTIGEN 6 COMPLEX, LOCUS E; LY6E *601385 : PUTATIVE PROSTATE CANCER TUMOR SUPPRESSOR #601386 : DEAFNESS, AUTOSOMAL RECESSIVE 12; DFNB12 *601387 : TUMOR SUSCEPTIBILITY GENE 101; TSG101 *601388 : DIABETES MELLITUS, INSULIN-DEPENDENT, 12; IDDM12 601389 : CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION 601390 : CEREBROFACIOARTICULAR SYNDROME *601391 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 13; SCYA13 *601392 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 14; SCYA14 *601393 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 15; SCYA15 *601394 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 16; SCYA16 *601395 : SMALL INDUCIBLE CYTOKINE A3-LIKE 1: SCYA3L1 *601396 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 8B; WNT8B *601397 : T BRACHYURY, MOUSE, HOMOLOG OF; T *601398 : VASCULAR ENDOTHELIAL GROWTH FACTOR B; VEGFB #601399 : PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY #601400 : SQUAMOUS CELL CARCINOMA, HEAD AND NECK *601401 : MYELOID LEUKEMIA FACTOR 2; MLF2 *601402 : MYELOID LEUKEMIA FACTOR 1; MLF1 *601403 : DEDICATOR OF CYTOKINESIS 1; DOCK1 *601404 : G PROTEIN-COUPLED RECEPTOR 68; GPR68 *601405 : CHYMOTRYPSIN C; CTRC *601406 : B-CELL CLL/LYMPHOMA 7A; BCL7A *601407 : DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2; NIDDM2 *601408 : ZINC FINGER PROTEIN 220; ZNF220 *601409 : HIV-1 TAT-INTERACTING PROTEIN; HTATIP *601410 : DIABETES MELLITUS, TRANSIENT NEONATAL *601411 : SARCOGLYCAN, DELTA; SGCD *601412 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 7; DFNA7 *601413 : DEIODINASE, IODOTHYRONINE, TYPE II; DIO2 *601414 : RETINITIS PIGMENTOSA 18; RP18 *601415 : V-MYB AVIAN MYELOBLASTOSIS VIRAL ONCOGENE HOMOLOG-LIKE 2; MYBL2 *601416 : KE4, MOUSE, HOMOLOG OF; HKE4 *601417 : 17-@BETA-HYDROXYSTEROID DEHYDROGENASE VIII; HSD17B8 *601418 : RIBOSOME BINDING PROTEIN 1; RRBP1 #601419 : DESMIN-RELATED MYOPATHY 601420 : MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE *601421 : LYSYL-tRNA SYNTHETASE; KARS *601422 : LEUCINE ZIPPER PROTEIN 1; LUZP1 *601423 : THYMINE-DNA GLYCOSYLASE; TDG ^601424 : MOVED TO 245050 *601425 : TRANSCRIPTION ELONGATION FACTOR A, 1; TCEA1 *601426 : NUCLEAR RECEPTOR SUBFAMILY 2, GROUP C, MEMBER 2; NR2C2 601427 : ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS *601428 : RNA, U4, SMALL NUCLEAR, AT-AC FORM *601429 : RNA, U6, SMALL NUCLEAR, AT-AC FORM *601430 : REGULATOR OF NONSENSE TRANSCRIPTS 1; RENT1 *601431 : TRANSFER RNA ALANINE; TRAN *601432 : TRANSFER RNA ARGININE 3; TRR3 *601433 : TRANSFER RNA METHIONINE 1; TRM1 *601434 : S-PHASE KINASE-ASSOCIATED PROTEIN 1A; SKP1A *601435 : S-PHASE KINASE-ASSOCIATED PROTEIN 1B; SKP1B *601436 : S-PHASE KINASE-ASSOCIATED PROTEIN 2; SKP2 *601437 : Fc FRAGMENT OF IgG, RECEPTOR TRANSPORTER, ALPHA; FCGRT 601438 : RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE 601439 : ATP-BINDING CASSETTE, SUBFAMILY C, MEMBER 9; ABCC9 *601440 : DIACYLGLYCEROL KINASE, EPSILON, 64-KD; DGKE *601441 : DIACYLGLYCEROL KINASE, ZETA, 104-KD: DGKZ *601442 : COFILIN 1; CFL1 *601443 : COFILIN 2; CFL2 *601444 : GENERAL CONTROL OF AMINO ACID SYNTHESIS, YEAST, HOMOLOG-LIKE 1; GCN5L1 *601445 : NADH-UBIQUINONE OXIDOREDUCTASE 1 BETA SUBCOMPLEX, 9; NDUFB9 601446 : SYNDACTYLY WITH RENAL AND ANOGENITAL MALFORMATIONS *601447 : UBIQUITIN-SPECIFIC PROTEASE 5; USP5 *601448 : NUCLEAR PROTEIN, ATAXIA-TELANGIECTASIA LOCUS; NPAT 601449 : DEAFNESS, PROGRESSIVE, WITH STAPES FIXATION 601450 : DISLOCATION OF THE HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERS AND FACIAL DYSMORPHISM 601451 : NEVO SYNDROME 601452 : OCULOAURICULOFRONTONASAL SYNDROME; OAFNS 601453 : TRICHODENTAL DYSPLASIA *601454 : PSORIASIS SUSCEPTIBILITY 3; PSORS3 #601455 : NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE *601456 : MULTIMERIN; MMRN #601457 : SEVERE COMBINED IMMUNODEFICIENCY, B CELL-NEGATIVE *601458 : INFLAMMATORY BOWEL DISEASE 2; IBD2 *601459 : PREPRONOCICEPTIN; PNOC *601460 : SOLUTE CARRIER FAMILY 21, MEMBER 2; SLC21A2 *601461 : ATONAL, DROSOPHILA, HOMOLOG OF, 1; ATOH1 #601462 : MYASTHENIC SYNDROME, SLOW-CHANNEL CONGENITAL; SCCMS *601463 : HYALURONAN SYNTHASE 1; HAS1 *601464 : LYMPHOID NUCLEAR PROTEIN RELATED TO AF4; LAF4 *601465 : DEOXYGUANOSINE KINASE; DGUOK 601466 : PATENT DUCTUS VENOSUS; PDV *601467 : MITOTIC ARREST-DEFICIENT 2, S. CEREVISIAE, HOMOLOG-LIKE 1; MAD2L1 *601468 : METHIONINE ADENOSYLTRANSFERASE II, ALPHA; MAT2A *601469 : PARATHYROID HORMONE RECEPTOR 2; PTHR2 *601470 : CHEMOKINE (C-X3-C) RECEPTOR 1; CX3CR1 *601471 : MOEBIUS SYNDROME 2; MBS2 *601472 : CHARCOT-MARIE-TOOTH DISEASE, NEURONAL TYPE, D *601473 : ZINC FINGER PROTEIN 75A; ZNF75A *601474 : ZINC FINGER PROTEIN 75C; ZNF75C *601475 : PERIODIC TRYPTOPHAN PROTEIN 2, YEAST, HOMOLOG OF; PWP2H *601476 : LYSOSOMAL-ASSOCIATED MULTISPANNING MEMBRANE PROTEIN 5; LAPTM5 601477 : RIBBING DISEASE *601478 : MYOSIN IA; MYO1A *601479 : MYOSIN IE; MYO1E *601480 : MYOSIN IF; MYO1F *601481 : MYOSIN X; MYO10 *601482 : DOWNREGULATOR OF TRANSCRIPTION 1, TBP-BINDING; DR1 *601483 : PATERNALLY EXPRESSED GENE 3; PEG3 *601484 : SELENOPROTEIN P, PLASMA, 1; SEPP1 *601485 : SYNTAXIN 1B; STX1B *601486 : DELETED IN AZOOSPERMIA-LIKE; DAZL *601487 : PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-GAMMA; PPARG *601488 : NEUTROPHIL CYTOSOLIC FACTOR 4; NCF4 *601489 : INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN, ACID-LABILE SUBUNIT; IGFALS *601490 : NUCLEAR FACTOR ERYTHROID 2, p45 SUBUNIT; NFE2 *601491 : IMPRINTED IN PRADER-WILLI SYNDROME; IPW #601492 : HYALURONIDASE DEFICIENCY *601493 : CARDIOMYOPATHY, DILATED, 1C; CMD1C #601494 : CARDIOMYOPATHY, DILATED, 1D; CMD1D #601495 : AGAMMAGLOBULINEMIA, NON-BRUTON TYPE *601496 : GDNF FAMILY RECEPTOR ALPHA-1; GFRA1 *601497 : BCL2-ASSOCIATED ATHANOGENE 1; BAG1 *601498 : PEROXISOME BIOGENESIS FACTOR 6; PEX6 *601499 : RIEGER SYNDROME, TYPE 2; RIEG2 *601500 : SMOOTHENED, DROSOPHILA, HOMOLOG OF; SMOH *601501 : MEM3, MOUSE, HOMOLOG OF *601502 : Fc FRAGMENT OF IgG, HIGH AFFINITY Ib, RECEPTOR FOR; FCGR1B *601503 : Fc FRAGMENT OF IgG, HIGH AFFINITY Ic, RECEPTOR FOR; FCGR1C *601504 : SEC14, S. CEREVISIAE, HOMOLOG-LIKE 1; SEC14L1 *601505 : ZINC FINGER PROTEIN 146; ZNF146 *601506 : NEURAL PRECURSOR CELL EXPRESSED, DEVELOPMENTALLY DOWNREGULATED 5; NEDD5 *601507 : CLATHRIN-ASSOCIATED/ASSEMBLY/ADAPTOR PROTEIN, SMALL 3, 22-KD; CLAPS3 #601508 : PARKINSON DISEASE, FAMILIAL, TYPE 1; PARK1 *601509 : GAMMA-GLUTAMYL HYDROLASE; GGH *601510 : SREBP CLEAVAGE-ACTIVATING PROTEIN *601511 : SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 5A; STAT5A *601512 : SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 6; STAT6 *601513 : FIBROBLAST GROWTH FACTOR 12; FGF12 *601514 : FIBROBLAST GROWTH FACTOR 11; FGF11 *601515 : FIBROBLAST GROWTH FACTOR 14; FGF14 *601516 : SPLICING FACTOR 1; SF1 *601517 : ATAXIN 2; ATX2 #601518 : PROSTATE CANCER, HEREDITARY, 1; HPC1 601519 : ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL F0 COMPLEX, SUBUNIT E; ATP5I *601520 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 17; SCYA17 *601521 : ENDOTHELIAL CELL-SPECIFIC MOLECULE 1; ESM1 *601522 : GROWTH FACTOR RECEPTOR-BOUND PROTEIN 7; GRB7 *601523 : GROWTH FACTOR RECEPTOR-BOUND PROTEIN 10; GRB10 *601524 : GROWTH FACTOR RECEPTOR-BOUND PROTEIN 14; GRB14 *601525 : CHITINASE 3-LIKE 1; CHI3L1 *601526 : CHITINASE 3-LIKE 2; CHI3L2 *601527 : CARTILAGE HOMEOPROTEIN 1; CART1 *601528 : VASCULAR ENDOTHELIAL GROWTH FACTOR C; VEGFC *601529 : NUCLEAR RECEPTOR SUBFAMILY 2, GROUP C, MEMBER 1; NR2C1 *601530 : SEQUESTOSOME 1; SQSTM1 *601531 : LEUKOTRIENE B4 RECEPTOR; LTB4R *601532 : CASPASE 6, APOPTOSIS-RELATED CYSTEINE PROTEASE; CASP6 *601533 : A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 2; ADAM2 *601534 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 3; KCNJ3 *601535 : EPHRIN A5; EFNA5 *601536 : NAVAJO BRAIN STEM SYNDROME *601537 : MICROCEPHALY, RETINITIS PIGMENTOSA, AND SUTURAL CATARACT *601538 : PROPHET OF PIT1, PAIRED-LIKE HOMEODOMAIN TRANSCRIPTION FACTOR; PROP1 #601539 : PEROXISOME BIOGENESIS DISORDERS; PBD *601540 : BROMODOMAIN-CONTAINING PROTEIN 2; BRD2 *601541 : BROMODOMAIN-CONTAINING PROTEIN 3; BRD3 *601542 : PAIRED-LIKE HOMEODOMAIN TRANSCRIPTION FACTOR 2; PITX2 #601543 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 8; DFNA8 #601544 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 3; DFNA3 *601545 : PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE, ISOFORM 1B, ALPHA SUBUNIT; PAFAH1B1 *601546 : PROSPERO-RELATED HOMEO BOX 1; PROX1 #601547 : CATARACT, CONGENITAL, CERULEAN TYPE, 2; CCA2 *601548 : EGF-CONTAINING FIBULIN-LIKE EXTRACELLULAR MATRIX PROTEIN 1; EFEMP1 *601549 : ALACRIMA *601550 : BLOOD GROUP SYSTEM SWANN *601551 : BLOOD GROUP SYSTEM FROESE *601552 : ECTOPIA LENTIS, SPONTANEOUS FILTERING BLEBS, AND CRANIOFACIAL DYSMORPHISM #601553 : HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD *601554 : T-COMPLEX-ASSOCIATED TESTIS EXPRESSED 1-LIKE 1; TCTEL1 *601555 : GTP-BINDING PROTEIN RHO7 *601556 : ATAXIN 1; ATX1 *601557 : ACETYL-CoA CARBOXYLASE-BETA; ACACB *601558 : RNA-BINDING PROTEIN GENE WITH MULTIPLE SPLICING *601559 : STUVE-WIEDEMANN SYNDROME 601560 : MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE 601561 : DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA *601562 : DYNEIN, CYTOPLASMIC, LIGHT CHAIN 601563 : HORNS IN SHEEP *601564 : PROTEASE, SERINE, 2; PRSS2 *601565 : INTERFERON CONSENSUS SEQUENCE-BINDING PROTEIN 1; ICSBP1 *601566 : INHIBITOR OF GROWTH 1; ING1 *601567 : LECTIN, MANNOSE-BINDING, 1; LMAN1 *601568 : ADDUCIN 3; ADD3 *601569 : UBIQUITIN-CONJUGATING ENZYME E2G; UBE2G *601570 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 7A; WNT7A *601571 : CAPPING PROTEIN, MUSCLE Z-LINE, ALPHA-2; CAPZA2 *601572 : CAPPING PROTEIN, MUSCLE Z-LINE, BETA; CAPZB *601573 : ENHANCER OF ZESTE, DROSOPHILA, HOMOLOG 2; EZH2 *601574 : TAF15 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 68-KD; TAF15 *601575 : FOS-LIKE ANTIGEN 2; FOSL2 *601576 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, SIGMA; PTPRS *601577 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, C POLYPEPTIDE-ASSOCIATED PROTEIN; PTPRCAP *601578 : CYCLIN G1; CCNG1 *601579 : ORNITHINE DECARBOXYLASE ANTIZYME 1; OAZ1 *601580 : CAPPING PROTEIN, MUSCLE Z-LINE, ALPHA-1; CAPZA1 *601581 : NEURONAL CELL ADHESION MOLECULE; NRCAM *601582 : INOSITOL POLYPHOSPHATE-5-PHOSPHATASE, 145-KD; INPP5D *601583 : WILMS TUMOR SUPPRESSOR LOCUS *601584 : PROTEIN-TYROSINE PHOSPHATASE, TYPE 4A, 2; PTP4A2 *601585 : PROTEIN-TYROSINE PHOSPHATASE, TYPE 4A, 1; PTP4A1 *601586 : PROSTAGLANDIN E RECEPTOR 4, EP4 SUBTYPE; PTGER4 *601587 : THYMOSIN, BETA-15 #601588 : EPIDERMAL DIFFERENTIATION COMPLEX; EDC *601589 : RAS p21 PROTEIN ACTIVATOR 2; RASA2 *601590 : ENVOPLAKIN; EVPL *601591 : PROTEIN KINASE, cGMP-DEPENDENT, TYPE II; PRKG2 *601592 : RECEPTOR-ASSOCIATED PROTEIN OF THE SYNAPSE, 43-KD; RAPSN *601593 : BRCA1-ASSOCIATED RING DOMAIN 1; BARD1 *601594 : JUMONJI; JMJ *601595 : MOTHERS AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 1; MADH1 *601596 : CHARCOT-MARIE-TOOTH NEUROPATHY, DEMYELINATING *601597 : B-CELL TRANSLOCATION GENE 2; BTG2 *601598 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, DELTA; PTPRD *601599 : SARCOSPAN; SSPN *601600 : ETS VARIANT GENE 5; ETV5 *601601 : TRANSCRIPTION FACTOR AP2-BETA; TFAP2B *601602 : TRANSCRIPTION FACTOR AP2-GAMMA; TFAP2C *601603 : LYMPHOCYTE CYTOSOLIC PROTEIN 2; LCP2 *601604 : INTERLEUKIN 12 RECEPTOR, BETA-1; IL12RB1 ^601605 : MOVED TO 601448 *601606 : TRICHOEPITHELIOMA, MULTIPLE FAMILIAL *601607 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY B, MEMBER 1; SMARCB1 601608 : SPASTIC PARAPLEGIA AND EVANS SYNDROME *601609 : L-3-@HYDROXYACYL-CoA DEHYDROGENASE, SHORT CHAIN; HADHSC *601610 : BUTYROPHILIN, SUBFAMILY 1, MEMBER A; BTN1A1 *601611 : SOLUTE CARRIER FAMILY 14, MEMBER 2; SLC14A2 *601612 : LUNG AGENESIS *601613 : BURKITT LYMPHOMA RECEPTOR 1; BLR1 601614 : NETRIN 1, MOUSE, HOMOLOG OF; NTN1 *601615 : ATP-BINDING CASSETTE, SUBFAMILY A, MEMBER 3; ABCA3 *601616 : IRIS PIGMENT EPITHELIUM ANOMALIES *601617 : RETINOL DEHYDROGENASE 5; RDH5 *601618 : SRY-BOX 18; SOX18 *601619 : RAL GUANINE NUCLEOTIDE DISSOCIATION STIMULATOR; RALGDS *601620 : T-BOX 5; TBX5 *601621 : T-BOX 3; TBX3 *601622 : TWIST, DROSOPHILA, HOMOLOG OF; TWIST *601623 : UBIQUITIN-PROTEIN LIGASE E3A; UBE3A *601624 : FICOLIN 2; FCN2 *601625 : ADP-RIBOSYLTRANSFERASE 1; ART1 #601626 : ACUTE MYELOGENOUS LEUKEMIA, FAMILIAL; AML *601627 : SURVIVAL OF MOTOR NEURON 2, CENTROMERIC; SMN2 601628 : MODIFIER OF VON WILLEBRAND FACTOR *601629 : PURKINJE CELL PROTEIN 4; PCP4 ^601630 : MOVED TO 600274 #601631 : IRIDOGONIODYSGENESIS, TYPE 1; IRID1 *601632 : POU DOMAIN, CLASS 4, TRANSCRIPTION FACTOR 1; POU4F1 *601633 : N-ETHYLMALEIMIDE-SENSITIVE FACTOR; NSF #601634 : NEURAL TUBE DEFECT, FOLATE-SENSITIVE 601635 : NEURAL TUBE DEFECT, FOLATE-RESISTANT *601636 : HYALURONAN SYNTHASE 2; HAS2 *601637 : CYTOCHROME P450, 51; CYP51 *601638 : PARTNER OF RAC1 *601639 : PROTEIN KINASE, cAMP-DEPENDENT, CATALYTIC, ALPHA; PRKACA ^601640 : MOVED TO 601314 *601641 : ACYL-CoA OXIDASE 2, BRANCHED-CHAIN; ACOX2 *601642 : INTERLEUKIN 12 RECEPTOR, BETA-2; IL12RB2 *601643 : PROTEIN PHOSPHATASE 2, REGULATORY SUBUNIT B (B56), ALPHA; PPP2R5A *601644 : PROTEIN PHOSPHATASE 2, REGULATORY SUBUNIT B (B56), BETA; PPP2R5B *601645 : PROTEIN PHOSPHATASE 2, REGULATORY SUBUNIT B (B56), GAMMA; PPP2R5C *601646 : PROTEIN PHOSPHATASE 2, REGULATORY SUBUNIT B (B56), DELTA; PPP2R5D *601647 : PROTEIN PHOSPHATASE 2, REGULATORY SUBUNIT B (B56), EPSILON; PPP2R5E *601648 : PROTEASOME 26S SUBUNIT, NON-ATPase, 4; PSMD4 ^601649 : MOVED TO 101400 *601650 : PARAGANGLIOMAS, FAMILIAL NONCHROMAFFIN, 2; PGL2 *601651 : NUCLEOSOME ASSEMBLY PROTEIN 1-LIKE 4; NAP1L4 *601652 : MYOCILIN; MYOC *601653 : EYES ABSENT 1; EYA1 *601654 : EYES ABSENT 2; EYA2 *601655 : EYES ABSENT 3; EYA3 *601656 : GATA-BINDING PROTEIN 6; GATA6 *601657 : DERMATAN SULFATE PROTEOGLYCAN 3; DSPG3 *601658 : OTOCONIN 90; OC90 *601659 : CHROMOSOME 21 OPEN READING FRAME 33; C21ORF33 ^601660 : MOVED TO 601150 *601661 : UBIQUITIN-CONJUGATING ENZYME E2I; UBE2I *601662 : ACTIVATED LEUKOCYTE CELL ADHESION MOLECULE; ALCAM *601663 : ESTROGEN RECEPTOR 2; ESR2 *601664 : U5 snRNP-SPECIFIC PROTEIN, 200-KD #601665 : OBESITY *601666 : DIABETES MELLITUS, INSULIN-DEPENDENT, 15; IDDM15 *601667 : ANGIOPOIETIN 1; ANGPT1 601668 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION ^601669 : MOVED TO 602229 *601670 : NEURO-D4 *601671 : REQUIEM, APOPTOSIS RESPONSE ZINC FINGER GENE; REQ *601672 : CER-D4 (MOUSE) HOMOLOG *601673 : EMBRYONIC LETHAL, ABNORMAL VISION, DROSOPHILA, HOMOLOG-LIKE 2; ELAVL2 *601674 : ENHANCER OF ZESTE, DROSOPHILA, HOMOLOG 1; EZH1 #601675 : TRICHOTHIODYSTROPHY; TTD *601676 : ACUTE INSULIN RESPONSE *601677 : NADH-UBIQUINONE OXIDOREDUCTASE 1 ALPHA SUBCOMPLEX, 5; NDUFA5 #601678 : BARTTER SYNDROME, ANTENATAL HYPERCALCIURIC FORM *601679 : GENERAL TRANSCRIPTION FACTOR II-I; GTF2I *601680 : ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE 2B; AMCD2B *601681 : PROTEASOME 26S SUBUNIT, ATPase, 5; PSMC5 *601682 : GLAUCOMA 1, OPEN ANGLE, C; GLC1C *601683 : COENZYME Q7; COQ7 *601684 : RIBOSOMAL PROTEIN S6 KINASE, 90-KD, 1; RPS6KA1 *601685 : RIBOSOMAL PROTEIN S6 KINASE, 90-KD, 2; RPS6KA2 *601686 : TELOMERASE PROTEIN COMPONENT 1; TEP1 *601687 : KERATIN 12; KRT12 *601688 : 15-@HYDROXYPROSTAGLANDIN DEHYDROGENASE; HPGD *601689 : TAF4B RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 105-KD; TAF4B *601690 : PHOSPHOLIPASE A2, GROUP VII; PLA2G7 *601691 : ATP-BINDING CASSETTE, SUBFAMILY A, MEMBER 4; ABCA4 *601692 : TRANSFORMING GROWTH FACTOR, BETA-INDUCED, 68-KD; TGFBI *601693 : UNCOUPLING PROTEIN 2; UCP2 *601694 : LEPTIN, SERUM LEVELS OF *601695 : CASEIN, KAPPA; CSN10 #601696 : NOVELTY SEEKING PERSONALITY TRAIT *601697 : PROTEASE INHIBITOR 8, OVALBUMIN TYPE; PI8 *601698 : ISLET CELL ANTIGEN-RELATED PROTEIN-TYROSINE PHOSPHATASE #601699 : PROSTAGLANDIN I2 SYNTHASE; PTGIS *601700 : SEBACEOUS GLAND HYPERPLASIA, FAMILIAL PRESENILE 601701 : ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA *601702 : RHO-ASSOCIATED COILED-COIL-CONTAINING PROTEIN KINASE 1; ROCK1 *601703 : VASODILATOR-STIMULATED PHOSPHOPROTEIN; VASP *601704 : MONOKINE INDUCED BY GAMMA INTERFERON; MIG #601705 : T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY #601706 : YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME 601707 : CRANIOFACIAL MALFORMATIONS, ASYMMETRIC, WITH POLYSYNDACTYLY AND ABNORMAL SKIN AND GUT DEVELOPMENT 601708 : SUPERIOR TRANSVERSE SCAPULAR LIGAMENT, CALCIFICATION OF, FAMILIAL *601709 : QUEBEC PLATELET DISORDER; QPD *601710 : EUKARYOTIC TRANSLATION INITIATION FACTOR 5; EIF5 *601711 : TNF RECEPTOR-ASSOCIATED FACTOR 1; TRAF1 *601712 : BACULOVIRAL IAP REPEAT-CONTAINING PROTEIN 2; BIRC2 *601713 : GLIA MATURATION FACTOR, BETA; GMFB *601714 : TEA DOMAIN FAMILY MEMBER 4; TEAD4 ^601715 : MOVED TO 601582 *601716 : STAUFEN, DROSOPHILA, HOMOLOG OF; STAU *601717 : SYNTAXIN-BINDING PROTEIN 2; STXBP2 #601718 : RETINITIS PIGMENTOSA 19; RP19 601719 : T-BOX 4 *601720 : ANTIGENIC DETERMINANT OF RECOMBINATION PROTEIN A, MOUSE, HOMOLOG OF; KIN *601721 : BACULOVIRAL IAP REPEAT-CONTAINING PROTEIN 3; BIRC3 ^601722 : MOVED TO 601712 *601723 : FRIZZLED, DROSOPHILA, HOMOLOG OF, 5; FZD5 *601724 : NEUROGENIC DIFFERENTIATION 1; NEUROD1 *601725 : NEUROGENIC DIFFERENTIATION 2; NEUROD2 *601726 : NEUROGENIN 1; NEUROG1 ^601727 : MOVED TO 601714 *601728 : PHOSPHATASE AND TENSIN HOMOLOG; PTEN *601729 : TEA DOMAIN FAMILY MEMBER 2; TEAD2 *601730 : PHOSPHATIDYLINOSITOL GLYCAN, CLASS C; PIGC *601731 : 5-@AMINOIMIDAZOLE-4-CARBOXAMIDE RIBONUCLEOTIDE FORMYLTRANSFERASE/IMP CYCLOHYDROLASE; ATIC *601732 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY C, MEMBER 1; SMARCC1 *601733 : GLUTATHIONE S-TRANSFERASE, MICROSOMAL, 2; MGST2 *601734 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY C, MEMBER 2; SMARCC2 *601735 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY D, MEMBER 1; SMARCD1 *601736 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY D, MEMBER 2; SMARCD2 *601737 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY D, MEMBER 3; SMARCD3 *601738 : EXOSTOSIN-LIKE 1; EXTL1 *601739 : MEIS1, MOUSE, HOMOLOG OF, 1; MEIS1 *601740 : MEIS1, MOUSE, HOMOLOG OF, 2; MEIS2 *601741 : CULLIN 5; CUL5 *601742 : KRAB-ASSOCIATED PROTEIN 1 *601743 : ONCOSTATIN M RECEPTOR; OSMR *601744 : SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 1; SLEB1 *601745 : POTASSIUM CHANNEL, SUBFAMILY K, MEMBER 1; KCNK1 *601746 : HYPOXIA UP-REGULATED 1; HYOU1 *601747 : ADP-RIBOSYLATION FACTOR DOMAIN PROTEIN 1; ARFD1 *601748 : GENERAL TRANSCRIPTION FACTOR IIH, POLYPEPTIDE 2; GTF2H2 *601749 : GLOMULIN *601750 : GENERAL TRANSCRIPTION FACTOR IIH, POLYPEPTIDE 3; GTF2H3 *601751 : G PROTEIN-COUPLED RECEPTOR 24; GPR24 *601752 : ECTONUCLEOSIDE TRIPHOSPHATE DIPHOSPHOHYDROLASE 2; ENTPD2 *601753 : PEPTIDYL-PROLYL ISOMERASE D; PPID *601754 : UBIQUITIN FUSION DEGRADATION 1-LIKE; UFD1L *601755 : DIGEORGE SYNDROME CRITICAL REGION GENE DGSI *601756 : UDP-N-ACETYL-ALPHA-D-GALACTOSAMINE:POLYPEPTIDE N-ACETYLGALACTOSAMINYLTRANSFERASE 3; GALNT3 *601757 : PEROXISOME BIOGENESIS FACTOR 7; PEX7 *601758 : PEROXISOME BIOGENESIS FACTOR 12; PEX12 601759 : PREAXIAL HALLUCAL POLYDACTYLY *601760 : GENERAL TRANSCRIPTION FACTOR IIH, POLYPEPTIDE 4; GTF2H4 *601761 : CASPASE 7, APOPTOSIS-RELATED CYSTEINE PROTEASE; CASP7 *601762 : CASPASE 10, APOPTOSIS-RELATED CYSTEINE PROTEASE; CASP10 *601763 : CASPASE 8, APOPTOSIS-RELATED CYSTEINE PROTEASE; CASP8 *601764 : BENIGN FAMILIAL INFANTILE CONVULSIONS ^601765 : MOVED TO 601542 *601766 : FRIZZLED, DROSOPHILA, HOMOLOG OF, 9; FZD9 *601767 : HUNTINGTIN-INTERACTING PROTEIN 1; HIP1 *601768 : SH3 DOMAIN, GRB2-LIKE, 1; SH3GL1 *601769 : VITAMIN D RECEPTOR; VDR *601770 : NEUROPEPTIDE Y RECEPTOR Y6; NPY6R *601771 : CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 1; CYP1B1 *601772 : H2AX HISTONE; H2AX *601773 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, N; PTPRN *601774 : ALPHA-1,6-@MANNOSYL-GLYCOPROTEIN BETA-1,6-N-ACETYLGLUCOSAMINYLTRANSFERASE; MGAT5 601775 : FOLATE LEVEL IN ERYTHROCYTES 601776 : ADDUCTED THUMB-CLUBFOOT SYNDROME #601777 : CONE-ROD DYSTROPHY 6; CORD6 *601778 : POLYMERASE, RNA, MITOCHONDRIAL; POLRMT 601779 : PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH SEVERE CARDIOMYOPATHY, AUTOSOMAL RECESSIVE #601780 : CEROID LIPOFUSCINOSIS, NEURONAL, LATE-INFANTILE, VARIANT *601781 : ZINC FINGER PROTEIN 45; ZNF45 *601782 : TESTIS-SPECIFIC PROTEIN KINASE 1; TESK1 601783 : STABLE TUBULE-ONLY POLYPEPTIDE *601784 : CATION CHANNEL, AMILORIDE-SENSITIVE, NEURONAL, 1; ACCN1 *601785 : PHOSPHOMANNOMUTASE 2; PMM2 *601786 : PHOSPHOMANNOMUTASE 1; PMM1 *601787 : TAF5 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 100-KD; TAF5 *601788 : GROWTH/DIFFERENTIATION FACTOR 8; GDF8 *601789 : PEROXISOME BIOGENESIS FACTOR 13; PEX13 *601790 : PANCREATIC POLYPEPTIDE RECEPTOR 1; PPYR1 *601791 : PEROXISOME BIOGENESIS FACTOR 14; PEX14 *601792 : PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 2; PPP1R2 ^601793 : MOVED TO 600724 *601794 : COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME *601795 : MITOGEN-ACTIVATED PROTEIN KINASE 3; MAPK3 *601796 : TAF4 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 135-KD; TAF4 *601797 : ABSENT IN MELANOMA 1; AIM1 *601798 : GLUCOSAMINE 6-PHOSPHATE DEAMINASE; GNPI *601799 : PROTEASE INHIBITOR 9, OVALBUMIN TYPE; PI9 *601800 : HAIR COLOR 3; HCL3 *601801 : TRANSCRIPTION FACTOR Sp2; SP2 *601802 : HOMEO BOX GENE EXPRESSED IN ES CELLS; HESX1 #601803 : PALLISTER-KILLIAN SYNDROME; PKS *601804 : TRANSCRIPTION FACTOR Sp3; SP3 *601805 : G PROTEIN-COUPLED RECEPTOR 30; GPR30 *601806 : MINICHROMOSOME MAINTENANCE, S. POMBE, HOMOLOG OF, 6; MCM6 *601807 : MATRIX METALLOPROTEINASE 19; MMP19 #601808 : CHROMOSOME 18q DELETION SYNDROME 601809 : SPONDYLOSPINAL THORACIC DYSOSTOSIS *601810 : DNA REPLICATION HELICASE, YEAST, HOMOLOG OF; DNA2L 601811 : PREMATURE AGING SYNDROME, OKAMOTO TYPE 601812 : PREMATURE AGING SYNDROME, PENTTINEN TYPE 601813 : EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL RECESSIVE *601814 : FXYD DOMAIN-CONTAINING ION TRANSPORT REGULATOR 2; FXYD2 #601815 : PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY 601816 : BILIRUBIN, ELEVATED CONCENTRATIONS OF, IN SERUM *601817 : NONMETASTATIC CELLS 3, PROTEIN EXPRESSED IN; NME3 *601818 : NONMETASTATIC CELLS 4, PROTEIN EXPRESSED IN; NME4 *601819 : FETAL ALZHEIMER ANTIGEN; FALZ #601820 : PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY *601821 : RNA, Y1 SMALL CYTOPLASMIC; RNY1 *601822 : RNA, Y3 SMALL CYTOPLASMIC; RNY3 *601823 : RNA, Y4 SMALL CYTOPLASMIC; RNY4 *601824 : RNA, Y5 SMALL CYTOPLASMIC; RNY5 *601825 : NADH-UBIQUINONE OXIDOREDUCTASE Fe-S PROTEIN 7; NDUFS7 *601826 : DIACYLGLYCEROL KINASE, DELTA, 130-KD; DGKD ^601827 : MOVED TO 601659 *601828 : NUCLEAR RECEPTOR SUBFAMILY 4, GROUP A, MEMBER 2; NR4A2 601829 : ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE ^601830 : MOVED TO 601770 *601831 : HISTONE 2B FAMILY, MEMBER Q; H2BFQ *601832 : RIBOSOMAL PROTEIN L29; RPL29 *601833 : ALLOGRAFT INFLAMMATORY FACTOR 1; AIF1 *601834 : CHEMOKINE (C-C) RECEPTOR 8; CCR8 *601835 : CHEMOKINE (C-C) RECEPTOR 6; CCR6 *601836 : KINESIN-ASSOCIATED PROTEIN 3; KIFAP3 *601837 : LIGASE IV, DNA, ATP-DEPENDENT; LIG4 *601838 : INOSITOL 1,3,4-TRISPHOSPHATE 5/6-KINASE; ITPK1 *601839 : EPHRIN RECEPTOR EphB3; EPHB3 ^601840 : MOVED TO 600286 *601841 : PROTEIN C INHIBITOR; PCI #601842 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 12; DFNA12 *601843 : SOLUTE CARRIER FAMILY 5 (SODIUM IODIDE SYMPORTER), MEMBER 5; SLC5A5 *601844 : PROTEIN KINASE, LYSINE-DEFICIENT 4; PRKWNK4 *601845 : GOOSECOID-LIKE; GSCL *601846 : VACUOLAR NEUROMYOPATHY #601847 : CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2; PFIC2 *601848 : MAS20P, S. CEREVISIAE, HOMOLOG OF 601849 : APLASIA/HYPOPLASIA OF PELVIS, FEMUR, FIBULA, AND ULNA WITH ABNORMAL DIGITS AND NAILS #601850 : RETINITIS PIGMENTOSA-DEAFNESS SYNDROME 1, AUTOSOMAL DOMINANT *601851 : CIRCADIAN LOCOMOTOR OUTPUT CYCLES KAPUT; CLOCK *601852 : INTERCELLULAR ADHESION MOLECULE 5; ICAM5 601853 : CEREBELLOTRIGEMINAL DERMAL DYSPLASIA *601854 : DIACYLGLYCEROL KINASE, GAMMA, 90-KD; DGKG *601855 : RHO GUANINE NUCLEOTIDE EXCHANGE FACTOR 1; ARHGEF1 *601856 : ZINC FINGER PROTEIN 211; ZNF211 ^601857 : MOVED TO 601056 601858 : CALMEGIN; CLGN #601859 : AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; ALPS *601860 : 17-@BETA-HYDROXYSTEROID DEHYDROGENASE IV; HSD17B4 *601861 : REGULATORY FACTOR X-ASSOCIATED PROTEIN; RFXAP *601862 : GLUCOSIDASE II, ALPHA SUBUNIT *601863 : REGULATORY FACTOR X, 5; RFX5 *601864 : GLUCOSIDASE II, BETA SUBUNIT *601865 : PROCOLLAGEN-LYSINE, 2-OXOGLUTARATE 5-DIOXYGENASE 2; PLOD2 *601866 : SEMAPHORIN 4D; SEMA4D *601867 : ATPase, Na+/K+ TRANSPORTING, BETA-3 POLYPEPTIDE; ATP1B3 #601868 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 13; DFNA13 *601869 : DEAFNESS, AUTOSOMAL RECESSIVE 15; DFNB15 *601870 : EUKARYOTIC INITIATION FACTOR 2-ASSOCIATED PROTEIN, 67-KD *601871 : CYSTEINE- AND GLYCINE-RICH PROTEIN 2; CSRP2 *601872 : SOLUTE CARRIER FAMILY 7, MEMBER 2; SLC7A2 *601873 : BETA-1,4-N-ACETYLGALACTOSAMINYLTRANSFERASE; GALGT *601874 : ELL-RELATED RNA POLYMERASE II, ELONGATION FACTOR; ELL2 ^601875 : MOVED TO 601630 601876 : SPERM-SPECIFIC ANTIGEN 1; SSFA1 *601877 : ENDOMETRIAL BLEEDING-ASSOCIATED FACTOR; EBAF *601878 : TRANSFORMING GROWTH FACTOR-BETA-INDUCIBLE EARLY GROWTH RESPONSE; TIEG *601879 : LECTIN, GALACTOSIDE-BINDING, SOLUBLE, 9; LGALS9 *601880 : SMALL INDUCIBLE CYTOKINE SUBFAMILY D, MEMBER 1; SCYD1 *601881 : RETINA AND ANTERIOR NEURAL FOLD GENE; RAX *601882 : DNA FRAGMENTATION FACTOR, 45-KD, ALPHA SUBUNIT; DFFA *601883 : DNA FRAGMENTATION FACTOR, 40-KD, BETA SUBUNIT; DFFB #601884 : HIGH BONE MASS; HBM #601885 : CATARACT, ZONULAR PULVERULENT 3; CZP3 *601886 : ACHAETE-SCUTE COMPLEX, DROSOPHILA, HOMOLOG-LIKE 2; ASCL2 #601887 : MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 5; MHS5 *601888 : MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 6; MHS6 *601889 : B-CELL CLL/LYMPHOMA 8; BCL8 *601890 : PROTEIN-TYROSINE KINASE PTK7; PTK7 *601891 : CYSTATIN 6; CST6 *601892 : KARYOPHERIN ALPHA-3; KPNA3 *601893 : TRIPLE FUNCTIONAL DOMAIN; TRIO *601894 : GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS *601895 : TNF RECEPTOR-ASSOCIATED FACTOR 2; TRAF2 *601896 : TNF RECEPTOR-ASSOCIATED FACTOR 3; TRAF3 *601897 : ZINC FINGER PROTEIN 148; ZNF148 *601898 : GROWTH HORMONE SECRETAGOGUE RECEPTOR; GHSR *601899 : SIGNAL-TRANSDUCING ADAPTOR MOLECULE 1; STAM *601900 : INTERFERON REGULATORY FACTOR 4; IRF4 *601901 : SOLUTE CARRIER FAMILY 8, MEMBER 2; SLC8A2 *601902 : ORIGIN RECOGNITION COMPLEX, SUBUNIT 1, S. CEREVISIAE, HOMOLOG OF; ORC1L *601903 : URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASE 2 FAMILY, MEMBER B17; UGT2B17 *601904 : RIBOSOMAL PROTEIN L39; RPL39 *601905 : RAB GERANYLGERANYL TRANSFERASE, ALPHA SUBUNIT; RABGGTA *601906 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 10B; WNT10B *601907 : NEOGENIN; NEO1 *601908 : G PROTEIN-COUPLED RECEPTOR 20; GPR20 *601909 : G PROTEIN-COUPLED RECEPTOR 21; GPR21 *601910 : G PROTEIN-COUPLED RECEPTOR 22; GPR22 *601911 : DISTAL-LESS HOMEO BOX 4; DLX4 *601912 : UBIQUITIN-LIKE 1; UBL1 *601913 : arsA ARSENITE TRANSPORTER, ATP-BINDING, E. COLI, HOMOLOG OF, 1; ASNA1 *601914 : PROLINE ARGININE-RICH END LEUCINE-RICH REPEAT PROTEIN; PRELP *601915 : TISSUE INHIBITOR OF METALLOPROTEINASE 4; TIMP4 *601916 : ARGININE-RICH, MUTATED IN EARLY STAGE TUMORS; ARMET *601917 : ALDEHYDE DEHYDROGENASE 3 FAMILY, MEMBER B2; ALDH3B2 *601918 : GROWTH/DIFFERENTIATION FACTOR 9; GDF9 *601919 : COAGULATION FACTOR II RECEPTOR-LIKE 2; F2RL2 *601920 : JAGGED 1; JAG1 ^601921 : MOVED TO 156535 *601922 : ANGIOPOIETIN 2; ANGPT2 ^601923 : MOVED TO 601124 *601924 : COATOMER PROTEIN COMPLEX, SUBUNIT ALPHA; COPA *601925 : RHO GDP-DISSOCIATION INHIBITOR ALPHA; ARHGDIA *601926 : THYROID HORMONE-RESPONSIVE SPOT14, RAT, HOMOLOG OF; THRSP 601927 : LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND FACIAL CHANGES *601928 : KERATIN, HAIR, BASIC, 6; KRTHB6 *601929 : ATPase, Ca(2+)-TRANSPORTING, UBIQUITOUS; ATP2A3 *601930 : BASONUCLIN; BNC *601931 : BCL2-LIKE 2; BCL2L2 *601932 : MUCIN 8, TRACHEOBRONCHIAL; MUC8 *601933 : CRYPTOCHROME 1; CRY1 *601934 : G PROTEIN PATHWAY SUPPRESSOR 1; GPS1 *601935 : G PROTEIN PATHWAY SUPPRESSOR 2; GPS2 *601936 : PRKC, APOPTOSIS, WT1, REGULATOR; PAWR *601937 : NUCLEAR RECEPTOR COACTIVATOR 3; NCOA3 ^601938 : MOVED TO 600523 *601939 : PROTEIN KINASE, SERINE/ARGININE-SPECIFIC, 1; SRPK1 *601940 : SPLICING FACTOR, ARGININE/SERINE-RICH, 4; SFRS4 *601941 : DIABETES MELLITUS, INSULIN-DEPENDENT, 6; IDDM6 *601942 : DIABETES MELLITUS, INSULIN-DEPENDENT, 10; IDDM10 *601943 : SPLICING FACTOR, ARGININE/SERINE-RICH, 9; SFRS9 *601944 : SPLICING FACTOR, ARGININE/SERINE-RICH, 6; SFRS6 *601945 : SPLICING FACTOR, ARGININE/SERINE-RICH, 8; SFRS8 ^601946 : MOVED TO 601531 *601947 : SRY-BOX 22; SOX22 ^601948 : MOVED TO 601784 *601949 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, BETA-4 SUBUNIT; CACNB4 *601950 : FRIEND OF GATA1 *601951 : CDC-LIKE KINASE 1; CLK1 601952 : KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA *601953 : CYCLIN H; CCNH #601954 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G; LGMD2G *601955 : CYCLIN-DEPENDENT KINASE 7; CDK7 *601956 : GDNF FAMILY RECEPTOR ALPHA-2; GFRA2 601957 : ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME *601958 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, BETA-3 SUBUNIT; CACNB3 *601959 : SERINE/THREONINE PROTEIN KINASE 2; STK2 *601960 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 20; SCYA20 *601961 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN METHYLTRANSFERASE 1-LIKE 1; HRMT1L1 *601962 : TAP-BINDING PROTEIN; TAPBP *601963 : TETRATRICOPEPTIDE REPEAT DOMAIN 1; TTC1 *601964 : DNAJ, E. COLI, HOMOLOG OF, SUBFAMILY C, MEMBER 7; DNAJC7 *601965 : ENDOTHELIAL DIFFERENTIATION GENE 3; EDG3 *601966 : REGULATORY SOLUTE CARRIER PROTEIN, FAMILY 1, MEMBER 1; RSC1A1 *601967 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 7B; WNT7B *601968 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 2B; WNT2B *601969 : DELETED IN MALIGNANT BRAIN TUMORS 1; DMBT1 *601970 : VASOACTIVE INTESTINAL PEPTIDE RECEPTOR 2; VIPR2 ^601971 : MOVED TO 600825 *601972 : RAR-RELATED ORPHAN RECEPTOR B; RORB *601973 : RETINOIC ACID RECEPTOR RESPONDER 2; RARRES2 *601974 : ENDOTHELIAL DIFFERENTIATION GENE 1; EDG1 *601975 : PLAKOPHILIN 1; PKP1 601976 : OTOFACIOOSSEOUS-GONADAL SYNDROME 601977 : THROMBOCYTOSIS, BENIGN FAMILIAL MICROCYTIC *601978 : SIGMA RECEPTOR, TYPE 1 601979 : HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION *601980 : LIPASE, GASTRIC; LIPF *601981 : RIBONUCLEASE A FAMILY, 6; RNASE6 *601982 : 8-@OXOGUANINE DNA GLYCOSYLASE; OGG1 *601983 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE KINASE 1; MAP4K1 *601984 : NUCLEAR RECEPTOR COACTIVATOR 4; NCOA4 *601985 : H4 GENE ^601986 : MOVED TO 601698 *601987 : CARNITINE PALMITOYLTRANSFERASE I, MUSCLE; CPT1B *601988 : LIM DOMAIN KINASE 2; LIMK2 *601989 : S100 CALCIUM-BINDING PROTEIN A13; S100A13 *601990 : TUMOR PROTEIN p73; TP73 *601991 : NEUROONCOLOGIC VENTRAL ANTIGEN 2; NOVA2 *601992 : FRIEDREICH ATAXIA 2 *601993 : NUCLEAR RECEPTOR COACTIVATOR 2; NCOA2 *601994 : TRANSFER RNA ARGININE *601995 : TENASCIN-R; TNR *601996 : PEPTIDE LN1 *601997 : BH3-INTERACTING DOMAIN DEATH AGONIST; BID *601998 : ESTROGEN-RELATED RECEPTOR, ALPHA; ESRRA *601999 : LIM HOMEO BOX GENE 1; LHX1 602000 : POLYMERASE I, RNA, POLYPEPTIDE B *602001 : NEUROPEPTIDE Y RECEPTOR Y5; NPY5R *602002 : ZYXIN; ZYX *602003 : LYMPHOID-RESTRICTED MEMBRANE PROTEIN; LRMP *602004 : PROTEIN-TYROSINE KINASE 6; PTK6 *602005 : SORTILIN-RELATED RECEPTOR; SORL1 *602006 : MITOGEN-ACTIVATED PROTEIN KINASE-ACTIVATED PROTEIN KINASE 2; MAPKAPK2 *602007 : V-CRK AVIAN SARCOMA VIRUS CT10 ONCOGENE HOMOLOG-LIKE; CRKL *602008 : KARYOPHERIN BETA-3; KPNB3 *602009 : CYTOCHROME c OXIDASE, SUBUNIT VIa, POLYPEPTIDE 2; COX6A2 *602010 : SPLICING FACTOR, ARGININE/SERINE-RICH, 11; SFRS11 *602011 : SUPPRESSOR OF TUMORIGENICITY 11; ST11 *602012 : ECTO NUCLEOSIDE TRIPHOSPHATE DIPHOSPHOHYDROLASE 2; ENTPD2 *602013 : POLYMERASE II, RNA, SUBUNIT G; POLR2G #602014 : HYPOMAGNESEMIA WITH SECONDARY HYPOCALCEMIA; HOMG *602015 : OUTER DENSE FIBER OF SPERM TAILS 2; ODF2 *602016 : KRUPPEL-LIKE FACTOR 2; KLF2 *602017 : PROTEASOME SUBUNIT, BETA-TYPE, 1; PSMB1 *602018 : NEURTURIN; NRTN *602019 : SQUALENE EPOXIDASE; SQLE *602020 : V-MAF AVIAN MUSCULOAPONEUROTIC FIBROSARCOMA ONCOGENE FAMILY, PROTEIN G; MAFG *602021 : PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 12A; PPP1R12A *602022 : MAL-LIKE; MALL *602023 : CHLORIDE CHANNEL, KIDNEY, B; CLCNKB *602024 : CHLORIDE CHANNEL, KIDNEY, A; CLCNKA *602025 : OBESITY QUANTITATIVE TRAIT LOCUS ON CHROMOSOME 20 *602026 : PHYTANOYL-CoA HYDROXYLASE; PHYH *602027 : TELOMERIC REPEAT-BINDING FACTOR 2; TERF2 ^602028 : MOVED TO 601900 602029 : BRAIN CYTOPLASMIC 1 *602030 : FUCOSYLTRANSFERASE 7; FUT7 *602031 : PROTEIN GERANYLGERANYLTRANSFERASE TYPE I, BETA SUBUNIT; PGGT1B 602032 : ECTODERMAL DYSPLASIA, 'PURE' HAIR-NAIL TYPE *602033 : ECHINODERM MICROTUBULE-ASSOCIATED PROTEIN-LIKE 1; EML1 *602034 : CORTICOTROPIN-RELEASING HORMONE RECEPTOR 2; CRHR2 *602035 : PROTEIN PHOSPHATASE 4, CATALYTIC SUBUNIT; PPP4C #602036 : ERYTHROKERATODERMIA, PROGRESSIVE SYMMETRIC *602037 : RAS HOMOLOG GENE FAMILY, MEMBER H; ARHH *602038 : DUAL-SPECIFICITY PHOSPHATASE 8; DUSP8 *602039 : EUKARYOTIC TRANSLATION INITIATION FACTOR 3, SUBUNIT 10; EIF3S10 *602040 : CELL ADHESION MOLECULE, NEURAL, 2; NCAM2 *602041 : HOMEO BOX 3A, NK; NKX3A *602042 : G PROTEIN-COUPLED RECEPTOR 18; GPR18 *602043 : G PROTEIN-COUPLED RECEPTOR 31; GPR31 *602044 : UNCOUPLING PROTEIN 3; UCP3 *602045 : RING FINGER PROTEIN 1; RING1 *602046 : GLUCOSE-REGULATED PROTEIN, 58-KD; GRP58 *602047 : PHOSPHODIESTERASE 3B, cGMP-INHIBITED; PDE3B *602048 : RAS-RELATED C3 BOTULINUM TOXIN SUBSTRATE 1; RAC1 *602049 : RAS-RELATED C3 BOTULINUM TOXIN SUBSTRATE 2; RAC2 *602050 : RAS-RELATED C3 BOTULINUM TOXIN SUBSTRATE 3; RAC3 *602051 : PEPTIDYL-PROLYL CIS/TRANS ISOMERASE, NIMA-INTERACTING, 1-LIKE; PIN1L *602052 : CYCLIN G-ASSOCIATED KINASE; GAK *602053 : CORE PROMOTER ELEMENT-BINDING PROTEIN; COPEB *602054 : T-BOX 1; TBX1 *602055 : INSULIN-INDUCED GENE 1; INSIG1 *602056 : DEFENSIN, BETA, 1; DEFB1 ^602057 : MOVED TO 300256 *602058 : PROTEASE INHIBITOR 10, OVALBUMIN TYPE; PI10 *602059 : IMMUNOGLOBULIN SUPERFAMILY CONTAINING LEUCINE-RICH REPEAT; ISLR *602060 : TRANSMEMBRANE PROTEASE, SERINE 2; TMPRSS2 *602061 : EPIREGULIN; EREG *602062 : NERVE INJURY-INDUCED PROTEIN 1; NINJ1 *602063 : TRANSALDOLASE 1; TALDO1 *602064 : MYO-INOSITOL MONOPHOSPHATASE 1; IMPA1 *602065 : ADENOSINE DEAMINASE, RNA-SPECIFIC, B2; ADARB2 *602066 : INFANTILE CONVULSIONS AND PAROXYSMAL CHOREOATHETOSIS, FAMILIAL; ICCA *602067 : CARDIOMYOPATHY, DILATED, 1F; CMD1F 602068 : LEISHMANIASIS, TEGUMENTARY *602069 : NEUROPILIN 1; NRP1 *602070 : NEUROPILIN 2; NRP2 *602071 : BROAD TERMINAL PHALANGES, FAMILIAL *602072 : CYTOCHROME c OXIDASE, SUBUNIT VIa, POLYPEPTIDE 1; COX6A1 *602073 : A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 3B; ADAM3B *602074 : DEATH-ASSOCIATED PROTEIN 3; DAP3 *602075 : SPECIAL AT-RICH SEQUENCE BINDING PROTEIN 1; SATB1 *602076 : TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY V, MEMBER 1; TRPV1 *602077 : ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 2; EEC2 #602078 : FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2; FEOM2 #602079 : TRIMETHYLAMINURIA #602080 : PAGET DISEASE OF BONE; PDB #602081 : SPECIFIC LANGUAGE IMPAIRMENT; SLI *602082 : CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE II; CDB2 #602083 : USHER SYNDROME, TYPE IF; USH1F *602084 : DELETED IN ENDOMETRIAL CARCINOMA *602085 : POLYDACTYLY, POSTAXIAL, TYPE A2 *602086 : ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3; ARVD3 *602087 : ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4 *602088 : NEPHRONOPHTHISIS 2; NPHP2 *602089 : HEMANGIOMA, CAPILLARY INFANTILE *602090 : LATENT TRANSFORMING GROWTH FACTOR-BETA-BINDING PROTEIN 3; LTBP3 *602091 : LATENT TRANSFORMING GROWTH FACTOR-BETA-BINDING PROTEIN 2; LTBP2 *602092 : DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 18; DFNB18 #602093 : CONE DYSTROPHY 3; COD3 ^602094 : MOVED TO 151660 *602095 : SOLUTE CARRIER FAMILY 30, MEMBER 4; SLC30A4 *602096 : ALZHEIMER DISEASE, FAMILIAL, TYPE 5 *602097 : USHER SYNDROME, TYPE IE; USH1E *602098 : POLO-LIKE KINASE; PLK *602099 : AMYOTROPHIC LATERAL SCLEROSIS 5; ALS5 *602100 : PBX/KNOTTED 1 HOMEO BOX 1; PKNOX1 *602101 : CLAUDIN 5; CLDN5 *602102 : SUPPRESSOR OF TY 5, S. CEREVISIAE, HOMOLOG OF; SUPT5H *602103 : TRANSMEMBRANE PROTEIN 1; TMEM1 *602104 : SH3 DOMAIN-BINDING PROTEIN 2; SH3BP2 *602105 : MutS, E. COLI, HOMOLOG OF, 4; MSH4 *602106 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 15; KCNJ15 602107 : NEUROPATHY, HEREDITARY THERMOSENSITIVE *602108 : MATRILIN 2; MATN2 *602109 : MATRILIN 3; MATN3 *602110 : SOLUTE CARRIER FAMILY 29 (NUCLEOSIDE TRANSPORTER), MEMBER 2; SLC29A2 *602111 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA, TYPE II *602112 : CHROMOSOME 22 OPEN READING FRAME 1; C22ORF1 *602113 : MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA 2; MLL2 602114 : NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVER DISEASE *602115 : FIBROBLAST GROWTH FACTOR 10; FGF10 *602116 : GLIOMA-AMPLIFIED SEQUENCE 41 *602117 : NECDIN; NDN *602118 : CHROMODOMAIN HELICASE DNA-BINDING PROTEIN 1; CHD1 *602119 : CHROMODOMAIN HELICASE DNA-BINDING PROTEIN 2; CHD2 *602120 : CHROMODOMAIN HELICASE DNA-BINDING PROTEIN 3; CHD3 *602121 : DIAPHANOUS, DROSOPHILA, HOMOLOG OF, 1; DIAPH1 *602122 : SIGNAL RECOGNITION PARTICLE, 72-KD; SRP72 *602123 : CALCIUM/CALMODULIN-DEPENDENT PROTEIN KINASE II-GAMMA; CAMKG *602124 : DYSTONIA 7, TORSION; DYT7 *602125 : CYTOCHROME c OXIDASE ASSEMBLY PROTEIN COX10; COX10 *602126 : ZINC FINGER PROTEIN 161, MOUSE, HOMOLOG OF; ZFP161 *602127 : SMOOTHELIN; SMTN *602128 : GAS2-RELATED ON CHROMOSOME 22 *602129 : MYOSIN IXB; MYO9B *602130 : MITOGEN-ACTIVATED PROTEIN KINASE-ACTIVATED PROTEIN KINASE 3; MAPKAPK3 *602131 : TUMOR-SUPPRESSING SUBCHROMOSOMAL TRANSFERABLE FRAGMENT cDNA 3; TSSC3 *602132 : MENINGIOMA-EXPRESSED ANTIGEN 6; MGEA6 *602133 : PHOSPHORIBOSYLFORMYLGLYCINAMIDINE SYNTHASE; PFAS *602134 : TREMOR, HEREDITARY ESSENTIAL, 2; ETM2 *602135 : INNER DYNEIN ARM, CHLAMYDOMONAS, HOMOLOG OF *602136 : PEROXISOME BIOGENESIS FACTOR 1; PEX1 *602137 : NADH-UBIQUINONE OXIDOREDUCTASE 1 ALPHA SUBCOMPLEX, 2; NDUFA2 *602138 : NADH-UBIQUINONE OXIDOREDUCTASE 1 ALPHA SUBCOMPLEX, 6; NDUFA6 *602139 : NADH-UBIQUINONE OXIDOREDUCTASE 1 ALPHA SUBCOMPLEX, 7; NDUFA7 *602140 : NADH-UBIQUINONE OXIDOREDUCTASE 1 BETA SUBCOMPLEX, 8; NDUFB8 *602141 : NADH-UBIQUINONE OXIDOREDUCTASE Fe-S PROTEIN 8; NDUFS8 *602142 : PHOSPHOLIPASE C, DELTA-1; PLCD1 *602143 : TUMOR PROTEIN p53-BINDING PROTEIN 2; TP53BP2 *602144 : BROMODOMAIN, TESTIS-SPECIFIC; BRDT *602145 : PROLIFERATION-ASSOCIATED 2G4, 38-KD; PA2G4 *602146 : LIM HOMEO BOX GENE 4 ^602147 : REMOVED FROM DATABASE *602148 : SRY-BOX 1; SOX1 *602149 : PAIRED-LIKE HOMEODOMAIN TRANSCRIPTION FACTOR 1; PITX1 *602150 : SNAIL, DROSOPHILA, HOMOLOG OF, 2; SNAI2 *602151 : DISHEVELLED 2; DVL2 602152 : RHYNS SYNDROME *602153 : KERATIN, HAIR, BASIC, 1; KRTHB1 *602154 : NONCODING TRANSCRIPT IN T CELLS *602155 : REPRODUCTION/CHROMOSOME 8; D8S2298E ^602156 : MOVED TO 601134 *602157 : NEUROONCOLOGIC VENTRAL ANTIGEN 1; NOVA1 *602158 : CHLORIDE CHANNEL, NUCLEOTIDE SENSITIVE, 1A; CLNS1A *602159 : CORONIN 2A; CORO2A *602160 : TRANSCRIPTION FACTOR DP2; TFDP2 *602161 : PROTEASOME ACTIVATOR SUBUNIT 2; PSME2 *602162 : SYNAPTONEMAL COMPLEX PROTEIN 1; SYCP1 *602163 : UBIQUITIN-CONJUGATING ENZYME E2E 2; UBE2E2 *602164 : 5-@HYDROXYTRYPTAMINE RECEPTOR 4; HTR4 *602165 : RET FINGER PROTEIN; RFP *602166 : ADAPTOR-RELATED PROTEIN COMPLEX 3, BETA-2 SUBUNIT; AP3B2 *602167 : ESTROGEN-RELATED RECEPTOR, BETA; ESRRB *602168 : VACCINIA-RELATED KINASE 1; VRK1 *602169 : VACCINIA-RELATED KINASE 2; VRK2 *602170 : MYELOID DIFFERENTIATION PRIMARY RESPONSE GENE 88; MYD88 *602171 : GLYCOPROTEIN A33; GPA33 *602172 : CYTOCHROME P450, SUBFAMILY VIIIB, POLYPEPTIDE 1; CYP8B1 *602173 : TRANSLOCATION PROTEIN 1, DROSOPHILA, HOMOLOG OF; TLOC1 *602174 : G PROTEIN-COUPLED RECEPTOR 25; GPR25 *602175 : PROTEASOME SUBUNIT, BETA-TYPE, 2; PSMB2 *602176 : PROTEASOME SUBUNIT, BETA-TYPE, 3; PSMB3 *602177 : PROTEASOME SUBUNIT, BETA-TYPE, 4; PSMB4 *602178 : CHONDROADHERIN; CHAD *602179 : HEAT-SHOCK 27-KD PROTEIN 2; HSPB2 *602180 : SIGNAL-INDUCED PROLIFERATION-ASSOCIATED GENE 1; SIPA1 *602181 : EBNA2 COACTIVATOR p100 *602182 : PHOSPHODIESTERASE I/NUCLEOTIDE PYROPHOSPHATASE 3; PDNP3 *602183 : BAGPIPE HOMEO BOX, DROSOPHILA, HOMOLOG OF, 1; BAPX1 *602184 : NADH-UBIQUINONE OXIDOREDUCTASE FLAVOPROTEIN 3; NDUFV3 ^602185 : MOVED TO 600004 *602186 : VGF, NERVE GROWTH FACTOR-INDUCIBLE; VGF *602187 : ZINC FINGER PROTEIN 195; ZNF195 *602188 : EPHRIN RECEPTOR EphA4; EPHA4 *602189 : REGULATOR OF G PROTEIN SIGNALING 3; RGS3 *602190 : EPHRIN RECEPTOR EphA7; EPHA7 *602191 : E74-LIKE FACTOR 3; ELF3 *602192 : A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 10; ADAM10 *602193 : SOLUTE CARRIER FAMILY 29 (NUCLEOSIDE TRANSPORTER), MEMBER 1; SLC29A1 *602194 : PROTEASE, SERINE, 11; PRSS11 *602195 : HEAT-SHOCK 27-KD PROTEIN 1; HSPB1 *602196 : PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES 602197 : CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 *602198 : CDK2-ASSOCIATED PROTEIN 1; CDK2AP1 *602199 : MEDIUM CHAIN 3-KETOACYL-CoA THIOLASE DEFICIENCY *602200 : VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY *602201 : EXTRACELLULAR MATRIX PROTEIN 1; ECM1 *602202 : DOLICHYL-DIPHOSPHOOLIGOSACCHARIDE-PROTEIN GLYCOSYLTRANSFERASE; DDOST *602203 : SARCOLIPIN; SLN *602204 : BICAUDAL-D, DROSOPHILA, HOMOLOG OF, 1; BICD1 ^602205 : MOVED TO 601805 602206 : RAS-ASSOCIATED PROTEIN RAB17 *602207 : RAS-ASSOCIATED PROTEIN RAB18; RAB18 *602208 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 10; KCNJ10 *602209 : RAS-RESPONSIVE ELEMENT BINDING PROTEIN 1; RREB1 *602210 : EUKARYOTIC TRANSLATION INITIATION FACTOR 3, SUBUNIT 6; EIF3S6 *602211 : FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 17; FKHL17 *602212 : SEVEN IN ABSENTIA, DROSOPHILA, HOMOLOG OF, 1; SIAH1 *602213 : SEVEN IN ABSENTIA, DROSOPHILA, HOMOLOG OF, 2; SIAH2 *602214 : CASEIN KINASE I, GAMMA-2; CSNK1G2 *602215 : DEFENSIN, BETA, 2; DEFB2 *602216 : SERINE/THREONINE PROTEIN KINASE 11; STK11 *602217 : SYNDECAN-BINDING PROTEIN; SDCBP *602218 : SAL-LIKE 1; SALL1 *602219 : SAL-LIKE 2; SALL2 *602220 : RAS-RELATED ON CHROMOSOME 22 *602221 : ZINC FINGER PROTEIN 198; ZNF198 *602222 : BENE PROTEIN *602223 : EUKARYOTIC TRANSLATION INITIATION FACTOR 4E-BINDING PROTEIN 1; EIF4EBP1 *602224 : EUKARYOTIC TRANSLATION INITIATION FACTOR 4E-BINDING PROTEIN 2; EIF4EBP2 *602225 : CONE-ROD HOMEO BOX-CONTAINING GENE; CRX *602226 : LYMPHOCYTE ANTIGEN 64, RADIOPROTECTIVE, 105-KD; LY64 *602227 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 19; SCYA19 *602228 : TRANSCRIPTION FACTOR 7-LIKE 2; TCF7L2 *602229 : SRY-BOX 10; SOX10 *602230 : SH3-BINDING DOMAIN AND GLUTAMIC ACID-RICH PROTEIN; SH3BGR *602231 : SMT3, YEAST, HOMOLOG 1; SMT3H1 *602232 : POTASSIUM CHANNEL, VOLTAGE-GATED, KQT-LIKE SUBFAMILY, MEMBER 3; KCNQ3 *602233 : APOPTOTIC PROTEASE ACTIVATING FACTOR 1; APAF1 *602234 : CASPASE 9, APOPTOSIS-RELATED CYSTEINE PROTEASE; CASP9 *602235 : POTASSIUM CHANNEL, VOLTAGE-GATED, KQT-LIKE SUBFAMILY, MEMBER 2; KCNQ2 ^602236 : MOVED TO 601880 ^602237 : MOVED TO 601470 *602238 : RIBOSOMAL RNA-PROCESSING PROTEIN 4, S. CEREVISIAE, HOMOLOG OF *602239 : CYTOCHROME P450, SUBFAMILY XXVIA, POLYPEPTIDE 1; CYP26A1 *602240 : ZINC FINGER PROTEIN 192; ZNF192 *602241 : MITOCHONDRIAL INTERMEDIATE PEPTIDASE; MIPEP *602242 : ADAPTOR-RELATED PROTEIN COMPLEX 2, SIGMA-1 SUBUNIT; AP2S1 *602243 : CD151 ANTIGEN; CD151 *602244 : DEOXYRIBONUCLEASE I-LIKE 3; DNASE1L3 *602245 : GTP-BINDING PROTEIN 1; GTPBP1 *602246 : ZINC FINGER PROTEIN 193; ZNF193 *602247 : XANTHOMATOSIS, SUSCEPTIBILITY TO *602248 : MALIGNANT ATROPHIC PAPULOSIS 602249 : PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES *602250 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 9; TNFRSF9 *602251 : TRANSLOCASE OF INNER MITOCHONDRIAL MEMBRANE 10, YEAST, HOMOLOG OF; TIMM10 602252 : MITOCHONDRIAL INTERMEMBRANE SPACE PROTEIN TIM12, YEAST, HOMOLOG OF *602253 : KRUPPEL-LIKE FACTOR 4; KLF4 *602254 : HEPATOCELLULAR CARCINOMA COMPLICATING HEMOCHROMATOSIS *602255 : SERINE/THREONINE PROTEIN KINASE 25; STK25 *602256 : PROTEIN PHOSPHATASE, EF-HAND CALCIUM-BINDING DOMAIN 2; PPEF2 *602257 : CD36 ANTIGEN-LIKE 2; CD36L2 ^602258 : MOVED TO 601040 *602259 : TETRATRICOPEPTIDE REPEAT DOMAIN 3; TTC3 *602260 : PERIOD, DROSOPHILA, HOMOLOG OF; PER1 *602261 : MATRIX METALLOPROTEINASE 15; MMP15 *602262 : MATRIX METALLOPROTEINASE 16; MMP16 ^602263 : MOVED TO 601807 *602264 : SPARC/OSTEONECTIN, CWCV, AND KAZAL-LIKE DOMAINS PROTEOGLYCAN; SPOCK *602265 : HUMAN ENHANCER OF FILAMENTATION 1 ^602266 : MOVED TO 300135 *602267 : A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 8; ADAM8 *602268 : AMINE OXIDASE, COPPER-CONTAINING, 2; AOC2 *602269 : ARMADILLO REPEAT GENE DELETED IN VCFS; ARVCF *602270 : ANTIOXIDANT PROTEIN 1; ATOX1 602271 : SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL *602272 : TRANSCRIPTION FACTOR 4; TCF4 *602273 : UDP-N-ACETYL-ALPHA-D-GALACTOSAMINE:POLYPEPTIDE N-ACETYLGALACTOSAMINYLTRANSFERASE 1; GALNT1 *602274 : UDP-N-ACETYL-ALPHA-D-GALACTOSAMINE:POLYPEPTIDE N-ACETYLGALACTOSAMINYLTRANSFERASE 2; GALNT2 *602275 : GUANYLATE CYCLASE ACTIVATOR 1B; GUCA1B *602276 : TRANSCRIPTIONAL ADAPTOR 2-LIKE; TADA2L *602277 : ZINC FINGER PROTEIN 184; ZNF184 *602278 : NEURAL PRECURSOR CELL EXPRESSED, DEVELOPMENTALLY DOWNREGULATED 4; NEDD4 *602279 : POLYADENYLATE-BINDING PROTEIN, NUCLEAR, 1; PABPN1 *602280 : TUBBY-LIKE PROTEIN 1; TULP1 *602281 : MILK FAT GLOBULE-EGF FACTOR 8; MFGE8 *602282 : ENDOTHELIAL DIFFERENTIATION GENE 2; EDG2 *602283 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 8; SCYA8 *602284 : BONE MORPHOGENETIC PROTEIN 8; BMP8 *602285 : MATRIX METALLOPROTEINASE 17; MMP17 *602286 : STEROL C5-DESATURASE-LIKE; SC5DL *602287 : CHROMOSOME 12 OPEN READING FRAME 8; C12ORF8 *602288 : RHOTEKIN; RTKN *602289 : DR1-ASSOCIATED PROTEIN 1; DRAP1 *602290 : TRIPARTITE MOTIF-CONTAINING PROTEIN 32; TRIM32 *602291 : FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 13; FKHL13 *602292 : ENOYL-CoA HYDRATASE, SHORT-CHAIN, 1, MITOCHONDRIAL; ECHS1 *602293 : CALCIUM- AND INTEGRIN-BINDING PROTEIN *602294 : HEPATOCYTE NUCLEAR FACTOR 3-ALPHA; HNF3A *602295 : HEPATOCYTE NUCLEAR FACTOR 3-GAMMA; HNF3G *602296 : ADAPTOR-RELATED PROTEIN COMPLEX 4, MU-1 SUBUNIT; AP4M1 *602297 : EPHRIN B3; EFNB3 *602298 : RAS-ASSOCIATED PROTEIN RAB7; RAB7 ^602299 : MOVED TO 300284 *602300 : 3-PRIME-@PHOSPHOADENYLYLSULFATE:GALACTOSYLCERAMIDE 3-PRIME-SULFOTRANSFERASE *602301 : GENERAL CONTROL OF AMINO ACID SYNTHESIS, YEAST, HOMOLOG-LIKE 2; GCN5L2 *602302 : HAIRLESS, MOUSE, HOMOLOG OF; HR *602303 : p300/CBP-ASSOCIATED FACTOR; PCAF *602304 : NUCLEAR RECEPTOR SUBFAMILY 1, GROUP D, MEMBER 2; NR1D2 ^602305 : MOVED TO 602162 *602306 : RAS-ASSOCIATED PROTEIN RAB2L; RAB2L *602307 : WW DOMAIN-CONTAINING PROTEIN 1 *602308 : WW DOMAIN-CONTAINING PROTEIN 2 *602309 : TUBBY-LIKE PROTEIN 2; TULP2 *602310 : RNA-BINDING MOTIF PROTEIN, SINGLE STRAND-INTERACTING, 1; RBMS1 *602311 : AGOUTI-RELATED PROTEIN, MOUSE, HOMOLOG OF; AGRP ^602312 : MOVED TO 142711 *602313 : OVO, DROSOPHILA, HOMOLOG-LIKE, 1; OVOL1 *602314 : LADININ 1; LAD1 *602315 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE 3; MAP2K3 *602316 : PHOSPHOLIPASE A2, LYSOSOMAL *602317 : SRC HOMOLOGY 3 AND CYSTEINE-RICH DOMAIN; STAC *602318 : TRANSCRIPTION TERMINATION FACTOR, MITOCHONDRIAL *602319 : NEL-LIKE 1; NELL1 *602320 : NEL-LIKE 2; NELL2 *602321 : GLUTATHIONE S-TRANSFERASE, KAPPA-1 *602322 : TELOMERASE RNA COMPONENT; TERC *602323 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 12; KCNJ12 *602324 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H3; HNRPH3 *602325 : EUKARYOTIC TRANSLATION INITIATION FACTOR 4-GAMMA, 2; EIF4G2 *602326 : RIBOSOMAL PROTEIN L23A; RPL23A *602327 : PLECKSTRIN-SEC7 DOMAINS PROTEIN; PSD ^602328 : MOVED TO 300118 *602329 : SUPPRESSOR OF LIN12-LIKE; SEL1L *602330 : ACTIN-BINDING LIM PROTEIN 1; ABLIM *602331 : ORIGIN RECOGNITION COMPLEX, SUBUNIT 5, S. CEREVISIAE, HOMOLOG OF; ORC5L *602332 : BARREN, DROSOPHILA, HOMOLOG OF, 1; BRRN1 *602333 : EPITHELIAL MEMBRANE PROTEIN 1; EMP1 *602334 : EPITHELIAL MEMBRANE PROTEIN 2; EMP2 *602335 : EPITHELIAL MEMBRANE PROTEIN 3; EMP3 *602336 : RECEPTOR TYROSINE KINASE-LIKE ORPHAN RECEPTOR 1; ROR1 *602337 : RECEPTOR TYROSINE KINASE-LIKE ORPHAN RECEPTOR 2; ROR2 *602338 : PRP4, YEAST, HOMOLOG OF *602339 : SOLUTE CARRIER FAMILY 15, MEMBER 2; SLC15A2 602340 : SENSORINEURAL HEARING LOSS, RETINAL PIGMENT EPITHELIUM LESIONS, DISCOLORED TEETH *602341 : FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 16; FKHL16 602342 : PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY *602343 : TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY C, MEMBER 1; TRPC1 *602344 : PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE 2; PAFAH2 *602345 : TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY C, MEMBER 3; TRPC3 *602346 : CONTACTIN-ASSOCIATED PROTEIN 1; CNTNAP1 #602347 : CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 3 *602348 : SMALL NUCLEAR RNA-ACTIVATING PROTEIN COMPLEX, POLYPEPTIDE 3; SNAPC3 *602349 : NETRIN 2, CHICKEN, HOMOLOG-LIKE; NTN2L *602350 : NEUROGRANIN; NRGN *602351 : CHEMOKINE-LIKE RECEPTOR 1; CMKLR1 *602352 : GONADOTROPIN-RELEASING HORMONE 2; GNRH2 *602353 : TRANSFORMING GROWTH FACTOR, BETA-1-INDUCED 1; TGFB1I1 *602354 : LINKER FOR ACTIVATION OF T CELLS; LAT *602355 : TNF RECEPTOR-ASSOCIATED FACTOR 6; TRAF6 *602356 : TNF RECEPTOR-ASSOCIATED FACTOR 5; TRAF5 *602357 : WISKOTT-ALDRICH SYNDROME PROTEIN-INTERACTING PROTEIN; WASPIP *602358 : HYPOCRETIN; HCRT *602359 : FXYD DOMAIN-CONTAINING ION TRANSPORT REGULATOR 1; FXYD1 *602360 : L-ARGININE:GLYCINE AMIDINOTRANSFERASE; GATM 602361 : GRACILE BONE DYSPLASIA *602362 : GTPase-ACTIVATING PROTEIN, RAN, 1; RANGAP1 ^602363 : MOVED TO 225500 *602364 : CATHEPSIN W; CTSW *602365 : CATHEPSIN C; CTSC *602366 : INTEGRIN-LINKED KINASE; ILK *602367 : PENTRAXIN I, NEURONAL; NPTX1 *602368 : GLUTAMATE RECEPTOR, IONOTROPIC, DELTA 2; GRID2 *602369 : CYSTEINE-RICH, ANGIOGENIC INDUCER, 61; CYR61 *602370 : GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED MOLECULE-LIKE PROTEIN; GML *602371 : FATTY ACID CoA LIGASE, LONG-CHAIN 3; FACL3 *602372 : ZONADHESIN; ZAN *602373 : CALPONIN 2; CNN2 *602374 : CALPONIN 3; CNN3 *602375 : MITOCHONDRIAL RIBOSOMAL PROTEIN L12; MRPL12 *602376 : INTERFERON, ALPHA, BETA, AND OMEGA, RECEPTOR 2; IFNAR2 *602377 : DYNAMIN 1; DNM1 *602378 : DYNAMIN 2; DNM2 ^602379 : MOVED TO 300141 *602380 : UROPLAKIN 1B; UPK1B *602381 : NGFIA-BINDING PROTEIN 2; NAB2 *602382 : PHOSPHOLIPASE D1, PHOSPHATIDYLCHOLINE-SPECIFIC; PLD1 *602383 : OSTEOGLYCIN; OGN *602384 : PHOSPHOLIPASE D2; PLD2 *602385 : SULFOTRANSFERASE FAMILY 1C, MEMBER 1; SULT1C1 *602386 : ZINC FINGER PROTEIN 212; ZNF212 *602387 : RNA-BINDING MOTIF PROTEIN, SINGLE STRAND-INTERACTING, 2; RBMS2 *602388 : SYMPLEKIN *602389 : Tu TRANSLATION ELONGATION FACTOR, MITOCHONDRIAL; TUFM *602390 : HEMOCHROMATOSIS, TYPE 2; HFE2 *602391 : PHOSPHATIDYLETHANOLAMINE N-METHYLTRANSFERASE; PEMT *602392 : HYPOCRETIN RECEPTOR 1; HCRTR1 *602393 : HYPOCRETIN RECEPTOR 2; HCRTR2 *602394 : NUCLEOLAR PROTEIN, 130-KD 602395 : GLYCEROL-3-PHOSPHATE ACYLTRANSFERASE, MITOCHONDRIAL *602396 : ANNEXIN A8; ANXA8 *602397 : ATPase, CLASS I, TYPE 8B, MEMBER 1; ATP8B1 #602398 : DESMOSTEROLOSIS *602399 : MITOGEN-ACTIVATED PROTEIN KINASE 12; MAPK12 602400 : ICHTHYOSIS, FOLLICULAR ATROPHODERMA, HYPOTRICHOSIS, AND HYPOHIDROSIS 602401 : ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL RECESSIVE *602402 : FORKHEAD BOX C2; FOXC2 *602403 : BLEOMYCIN HYDROLASE; BLMH *602404 : PARKINSON DISEASE 3 ^602405 : MOVED TO 600910 *602406 : HEART- AND NEURAL CREST DERIVATIVES-EXPRESSED 1; HAND1 *602407 : HEART- AND NEURAL CREST DERIVATIVES-EXPRESSED 2; HAND2 *602408 : NUCLEAR RECEPTOR SUBFAMILY 1, GROUP D, MEMBER 1; NR1D1 *602409 : MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 10; MLLT10 *602410 : BROMODOMAIN AND PHD FINGER-CONTAINING PROTEIN; BRPF1 *602411 : EXOSTOSIN-LIKE 2; EXTL2 *602412 : RIBOSOMAL PROTEIN S24; RPS24 *602413 : SUCCINATE DEHYDROGENASE COMPLEX, SUBUNIT C, INTEGRAL MEMBRANE PROTEIN, 15-KD; SDHC *602414 : AMYLOID BETA A4 PRECURSOR PROTEIN-BINDING, FAMILY A, MEMBER 1; APBA1 *602415 : DYSTROBREVIN, BETA; DTNB *602416 : ADAPTOR-RELATED PROTEIN COMPLEX 3, SIGMA-2 SUBUNIT; AP3S2 ^602417 : MOVED TO 602974 602418 : WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME *602419 : EARLY GROWTH RESPONSE 3; EGR3 *602420 : POTASSIUM CHANNEL, VOLTAGE-GATED, SHAKER-RELATED SUBFAMILY, MEMBER 10; KCNA10 *602421 : CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR *602422 : STEM-LOOP BINDING PROTEIN; SLBP *602423 : NUCLEAR RECEPTOR SUBFAMILY 1, GROUP H, MEMBER 3; NR1H3 *602424 : DOUBLESEX- AND MAB-3-RELATED TRANSCRIPTION FACTOR 1; DMRT1 *602425 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 4; MAP3K4 *602426 : NUCLEAR VALOSIN-CONTAINING PROTEIN-LIKE; NVL *602427 : T-BOX 6; TBX6 *602428 : HYALURONAN SYNTHASE 3; HAS3 *602429 : GLAUCOMA 1, OPEN ANGLE, D; GLC1D *602430 : ROUNDABOUT, DROSOPHILA, HOMOLOG OF, 1; ROBO1 *602431 : ROUNDABOUT, DROSOPHILA, HOMOLOG OF, 2; ROBO2 *602432 : OPTINEURIN; OPTN *602433 : AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4 *602434 : ANCIENT UBIQUITOUS PROTEIN 1; AUP1 *602435 : PEPTIDYL-PROLYL ISOMERASE E; PPIE *602436 : MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I CHAIN-RELATED GENE B; MICB *602437 : GTP CYCLOHYDROLASE I FEEDBACK REGULATORY PROTEIN; GCHFR *602438 : HEAT-SHOCK TRANSCRIPTION FACTOR 4; HSF4 *602439 : ACUTE MYELOGENOUS LEUKEMIA *602440 : AMYOTROPHY, MONOMELIC *602441 : CYTOKINE-INDUCIBLE SH2-CONTAINING PROTEIN; CISH *602442 : INTERSECTIN 1; ITSN1 *602443 : X-PROLYL AMINOPEPTIDASE-LIKE; XPNPEPL *602444 : TRANSCRIPTION FACTOR 17; TCF17 *602445 : PROTEASE INHIBITOR 12; PI12 *602446 : GLYPICAN 5; GPC5 *602447 : PARAOXONASE 2; PON2 *602448 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 5; MAP3K5 *602449 : A-KINASE ANCHOR PROTEIN 1; AKAP1 #602450 : SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION *602451 : PYRIMIDINERGIC RECEPTOR P2Y, G PROTEIN-COUPLED, 6; P2RY6 *602452 : BUDDING UNINHIBITED BY BENZIMIDAZOLES 1, S. CEREVISIAE, HOMOLOG OF; BUB1 *602453 : INTEGRIN, ALPHA-D; ITGAD *602454 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, U; PTPRU 602455 : REGENERATION-ASSOCIATED SERPIN-1 ^602456 : REMOVED FROM DATABASE *602457 : FAS-ASSOCIATED VIA DEATH DOMAIN; FADD *602458 : SORTILIN; SORT1 #602459 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 15; DFNA15 *602460 : POU DOMAIN, CLASS 4, TRANSCRIPTION FACTOR 3; POU4F3 *602461 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR TYPE, SUBSTRATE 1; PTPNS1 *602462 : COLLAPSIN RESPONSE MEDIATOR PROTEIN 1; CRMP1 *602463 : DIHYDROPYRIMIDINASE-LIKE 2; DPYSL2 *602464 : TNF RECEPTOR-ASSOCIATED FACTOR 4; TRAF4 *602465 : SPROUTY, DROSOPHILA, HOMOLOG OF, 1; SPRY1 *602466 : SPROUTY, DROSOPHILA, HOMOLOG OF, 2; SPRY2 *602467 : SPROUTY, DROSOPHILA, HOMOLOG OF, 3; SPRY3 *602468 : NEURABIN I *602469 : FOLATE RECEPTOR 3; FOLR3 *602470 : PROSTATE STEM CELL ANTIGEN 602471 : SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, SKELETAL ABNORMALITIES 602472 : CREASES, INFRA-AURICULAR CUTANEOUS, WITH TALL STATURE AND ADVANCED BONE AGE *602473 : ENCEPHALOPATHY, ETHYLMALONIC *602474 : CDC2-INHIBITORY KINASE, MEMBRANE-ASSOCIATED AND TYROSINE/THREONINE-SPECIFIC, 1 #602475 : OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE; OPLL *602476 : FEBRILE CONVULSIONS, FAMILIAL, 1; FEB1 *602477 : FEBRILE CONVULSIONS, FAMILIAL, 2; FEB2 *602478 : DNA METHYLTRANSFERASE 2; DNMT2 *602479 : POU DOMAIN, CLASS 3, TRANSCRIPTION FACTOR 1; POU3F1 *602480 : POU DOMAIN, CLASS 3, TRANSCRIPTION FACTOR 3; POU3F3 *602481 : MIGRAINE, FAMILIAL HEMIPLEGIC, 2; MHP2 *602482 : AXENFELD-RIEGER ANOMALY WITH ATRIAL SEPTAL DEFECT AND SENSORINEURAL HEARING LOSS 602483 : EARS, PROMINENT AND CONSTRICTED 602484 : PELVIC HYPOPLASIA WITH LOWER-LIMB ARTHROGRYPOSIS #602485 : HYPERINSULINISM, AUTOSOMAL DOMINANT *602486 : PROCESSING OF PRECURSOR RNAs *602487 : PERCHLORIC ACID-SOLUBLE PROTEIN, 14.5-KD *602488 : PLECKSTRIN HOMOLOGY, SEC7, AND COILED-COIL DOMAINS PROTEIN 2; PSCD2 *602489 : GAP-ASSOCIATED TYROSINE PHOSPHOPROTEIN, 62-KD *602490 : NUCLEAR RECEPTOR-INTERACTING PROTEIN 1; NRIP1 *602491 : HYPERLIPIDEMIA, COMBINED, 1 *602492 : PENTRAXIN 3; PTX3 *602493 : UV RADIATION RESISTANCE-ASSOCIATED GENE; UVRAG *602494 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 23; SCYA23 *602495 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 24; SCYA24 *602496 : MERCAPTOPYRUVATE SULFURTRANSFERASE; MPST 602497 : CHONDRODYSPLASIA PUNCTATA, BRACHYTELEPHALANGIC *602498 : TRK-FUSED GENE; TFG 602499 : MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA *602500 : GOLGI AUTOANTIGEN, GOLGIN SUBFAMILY B, 1; GOLGB1 602501 : MEGALENCEPHALY-CUTIS MARMORATA TELANGIECTATICA CONGENITA *602502 : GOLGI AUTOANTIGEN, GOLGIN SUBFAMILY A, 1; GOLGA1 *602503 : FREQUENTLY REARRANGED IN ADVANCED T-CELL LYMPHOMAS; FRAT1 *602504 : SHORT STATURE HOMEO BOX 2; SHOX2 *602505 : PAXILLIN; PXN *602506 : CYCLIN T1; CCNT1 *602507 : ZINC FINGER PROTEIN 103, MOUSE, HOMOLOG OF; ZFP103 *602508 : PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE, ISOFORM 1B, BETA SUBUNIT; PAFAH1B2 *602509 : GOLGI AUTOANTIGEN, GOLGIN SUBFAMILY A, 4; GOLGA4 *602510 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, H; PTPRH 602511 : PSEUDOACROMEGALY WITH SEVERE INSULIN RESISTANCE *602512 : REGULATOR OF G PROTEIN SIGNALING 12; RGS12 *602513 : REGULATOR OF G PROTEIN SIGNALING 14; RGS14 *602514 : REGULATOR OF G PROTEIN SIGNALING 16; RGS16 *602515 : PHOSPHOLIPASE D1, GLYCOSYLPHOSPHATIDYLINOSITOL-SPECIFIC; GPLD1 *602516 : REGULATOR OF G PROTEIN SIGNALING 4; RGS4 *602517 : REGULATOR OF G PROTEIN SIGNALING 7; RGS7 *602518 : LECTIN, GALACTOSIDE-BINDING, SOLUBLE, 4; LGALS4 *602519 : UBIQUITIN-SPECIFIC PROTEASE 7; USP7 *602520 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE 5; MAP2K5 *602521 : MITOGEN-ACTIVATED PROTEIN KINASE 7; MAPK7 #602522 : BARTTER SYNDROME, INFANTILE, WITH SENSORINEURAL DEAFNESS *602523 : DOWN SYNDROME CELL ADHESION MOLECULE; DSCAM *602524 : PYRUVATE DEHYDROGENASE KINASE, ISOENZYME 1; PDK1 *602525 : PYRUVATE DEHYDROGENASE KINASE, ISOENZYME 2; PDK2 *602526 : PYRUVATE DEHYDROGENASE KINASE, ISOENZYME 3; PDK3 *602527 : PYRUVATE DEHYDROGENASE KINASE, ISOENZYME 4; PDK4 *602528 : TUBULIN, ALPHA-2; TUBA2 *602529 : TUBULIN, ALPHA, BRAIN-SPECIFIC *602530 : TUBULIN, ALPHA, UBIQUITOUS 602531 : ARTERIAL OCCLUSIVE DISEASE, PROGRESSIVE, WITH HYPERTENSION, HEART DEFECTS, BONE FRAGILITY, AND BRACHYSYNDACTYLY *602532 : SIX-TWELVE LEUKEMIA GENE *602533 : ONCOGENE DJ1 *602534 : SYNAPTOSOMAL-ASSOCIATED PROTEIN, 23-KD; SNAP23 602535 : MARSHALL-SMITH SYNDROME *602536 : RAB3 GTPase-ACTIVATING PROTEIN *602537 : CALPAIN 5; CAPN5 *602538 : CUG TRIPLET REPEAT, RNA-BINDING PROTEIN 2; CUGBP2 *602539 : MITOGEN-ACTIVATED KINASE KINASE KINASE 3; MAP3K3 602540 : ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS 602541 : MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE *602542 : BASIC TRANSCRIPTION FACTOR 3; BTF3 *602543 : BASIC TRANSCRIPTION FACTOR 3-LIKE 1; BTF3L1 *602544 : PARKIN; PARK2 *602545 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, KAPPA; PTPRK *602546 : SIALYLTRANSFERASE 8B; SIAT8B *602547 : POLYSIALYLTRANSFERASE; PST *602548 : OPIOID RECEPTOR-LIKE 1; OPRL1 *602549 : PROTEIN KINASE C-LIKE 2; PRKCL2 *602550 : ARYL HYDROCARBON RECEPTOR NUCLEAR TRANSLOCATOR-LIKE; ARNTL 602551 : JEJUNAL ATRESIA WITH RENAL ADYSPLASIA *602552 : NUCLEOPORIN, 88-KD; NUP88 602553 : ANAL ATRESIA, HYPOSPADIAS, AND PENOSCROTAL INVERSION 602554 : TORSION DYSTONIA WITH ONSET IN INFANCY 602555 : MICROCEPHALY, MACROTIA, AND MENTAL RETARDATION 602556 : FACIAL DYSMORPHISM, CLEFT PALATE, HEARING LOSS, AND CAMPTODACTYLY 602557 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE 602558 : CRANIOMICROMELIC SYNDROME *602559 : EXPORTIN 1; XPO1 *602560 : TRACHEAL ANTIMICROBIAL PEPTIDE 602561 : BRACHYDACTYLY, INTRAVENTRICULAR SEPTAL DEFECT, AND DEAFNESS 602562 : MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA *602563 : HOMEO BOX 6A, NK; NKX6A 602564 : EMPHYSEMA, CONGENITAL, WITH DEAFNESS, PENOSCROTAL WEB, AND MENTAL RETARDATION *602565 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 25; SCYA25 *602566 : PURINERGIC RECEPTOR P2X, LIGAND-GATED ION CHANNEL, 7; P2RX7 *602567 : LIM AND SENESCENT CELL ANTIGEN-LIKE DOMAINS 1; LIMS1 *602568 : METHIONINE SYNTHASE REDUCTASE; MTRR *602569 : SYNUCLEIN, BETA; SNCB *602570 : JAGGED 2; JAG2 *602571 : RNA-BINDING MOTIF PROTEIN 4; RBM4 *602572 : ANNEXIN A11; ANXA11 *602573 : ANNEXIN A13; ANXA13 *602574 : TECTORIN, ALPHA; TECTA *602575 : LIM HOMEO BOX TRANSCRIPTION FACTOR 1, BETA; LMX1B *602576 : LUNATIC FRINGE; LFNG *602577 : MANIC FRINGE; MFNG *602578 : RADICAL FRINGE; RFNG #602579 : CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib *602580 : GOLGI AUTOANTIGEN, GOLGIN SUBFAMILY A, 2; GOLGA2 *602581 : GOLGI AUTOANTIGEN, GOLGIN SUBFAMILY A, 3; GOLGA3 *602582 : DELTEX, DROSOPHILA, HOMOLOG OF, 1; DTX1 *602583 : G PROTEIN-COUPLED RECEPTOR 37; GPR37 *602584 : RETICULOCALBIN 2; RCN2 602585 : MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE 602586 : ACYL-CoA THIOESTER HYDROLASE, LONG-CHAIN, 1 602587 : ACYL-CoA THIOESTER HYDROLASE, LONG-CHAIN, 2 #602588 : BRANCHIOOTIC SYNDROME *602589 : FUCOSYLTRANSFERASE 8; FUT8 *602590 : p21/CDC42/RAC1-ACTIVATED KINASE 1; PAK1 *602591 : KINESIN, HEAVY CHAIN, 2; KIF2 *602592 : LYMPHOCYTE ANTIGEN CD5-LIKE; CD5L *602593 : CORNEODESMOSIN; CDSN *602594 : RETINITIS PIGMENTOSA 22; RP22 *602595 : SMN-INTERACTING PROTEIN 1; SIP1 602596 : PANCREATIC LYMPHOMA, FAMILIAL *602597 : B-CELL CLL/LYMPHOMA 9; BCL9 *602598 : PROSTAGLANDIN D2 SYNTHASE, HEMATOPOIETIC ^602599 : MOVED TO 602631 *602600 : LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 8; LRP8 *602601 : LOW DENSITY LIPOPROTEIN, OXIDIZED, RECEPTOR 1; OLR1 *602602 : SECRETED AND TRANSMEMBRANE 1; SECTM1 *602603 : MAGO NASHI, DROSOPHILA, HOMOLOG OF; MAGOH *602604 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, INHIBITOR 1; KCNJN1 ^602605 : MOVED TO 602221 602606 : COCAINE- AND AMPHETAMINE-REGULATED TRANSCRIPT *602607 : SOLUTE CARRIER FAMILY 22, MEMBER 1; SLC22A1 *602608 : SOLUTE CARRIER FAMILY 22, MEMBER 2; SLC22A2 *602609 : PHOSPHATIDYLINOSITOL 3-KINASE, CLASS 3; PIK3C3 *602610 : PHOSPHATIDYLINOSITOL 3-KINASE, REGULATORY, 4; PIK3R4 602611 : SPONDYLOEPIPHYSEAL DYSPLASIA WITH CORONAL CRANIOSYNOSTOSIS, CATARACTS, CLEFT PALATE, AND MENTAL RETARDATION 602612 : CAMPTODACTYLY, MYOPIA, AND FIBROSIS OF THE MEDIAL RECTUS MUSCLE OF EYE 602613 : SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL *602614 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 7; MAP3K7 *602615 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 7-INTERACTING PROTEIN 1; MAP3K7IP1 *602616 : ALPHA-1,6-@MANNOSYL-GLYCOPROTEIN BETA-1,2-N-ACETYLGLUCOSAMINYLTRANSFERASE; MGAT2 *602617 : FORKHEAD BOX E1; FOXE1 *602618 : C-TERMINAL-BINDING PROTEIN 1; CTBP1 *602619 : C-TERMINAL-BINDING PROTEIN 2; CTBP2 *602620 : LEGUMAIN; LGMN *602621 : COXSACKIE VIRUS AND ADENOVIRUS RECEPTOR; CXADR *602622 : DEOXYRIBONUCLEASE I-LIKE 2; DNASE1L2 *602623 : FK506-BINDING PROTEIN 5; FKBP5 ^602624 : MOVED TO 602570 *602625 : BAI1-ASSOCIATED PROTEIN 1; BAIAP1 *602626 : INTERLEUKIN 1 RECEPTOR ACCESSORY PROTEIN; IL1RAP *602627 : CELL DIVISION CYCLE 18, S. POMBE, HOMOLOG-LIKE; CDC18L *602628 : CHECKPOINT SUPPRESSOR 1; CHES1 *602629 : DYSTONIA 6, TORSION; DYT6 *602630 : TG-INTERACTING FACTOR; TGIF *602631 : SOLUTE CARRIER FAMILY 22 (ORGANIC CATION TRANSPORTER), MEMBER 1-LIKE; SLC22A1L *602632 : PODOCALYXIN-LIKE; PODXL *602633 : FOUR-AND-A-HALF LIM DOMAINS 2; FHL2 *602634 : DNAJ, E. COLI, HOMOLOG OF, SUBFAMILY B, MEMBER 9; DNAJB9 *602635 : SUPPRESSIN *602636 : PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 8; PPP1R8 *602637 : SECRETED PHOSPHOPROTEIN 2, 24-KD; SPP2 *602638 : MINICHROMOSOME MAINTENANCE, S. CEREVISIAE, HOMOLOG OF, 4; MCM4 *602639 : HYPODONTIA, AUTOSOMAL RECESSIVE; HYD2 *602640 : ILEAL DIPEPTIDYLPEPTIDASE *602641 : EUKARYOTIC TRANSLATION INITIATION FACTOR 4A, ISOFORM 1; EIF4A1 *602642 : TUMOR NECROSIS FACTOR LIGAND SUPERFAMILY, MEMBER 11; TNFSF11 *602643 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 11B; TNFRSF11B *602644 : TRANSMEMBRANE 4 SUPERFAMILY, MEMBER 7; TM4SF7 *602645 : SEMAPHORIN 3C; SEMA3C *602646 : G PROTEIN-COUPLED RECEPTOR 35; GPR35 *602647 : NUCLEAR RNA EXPORT FACTOR 1; NXF1 *602648 : CHEMOKINE-BINDING PROTEIN 2; CCBP2 *602649 : COLD-INDUCIBLE RNA-BINDING PROTEIN; CIRBP *602650 : SPECKLE-TYPE POZ PROTEIN; SPOP *602651 : NARDILYSIN; NRD1 *602652 : KALLIKREIN 6; KLK6 *602653 : TECTORIN, BETA; TECTB *602654 : FERM, ARHGEF, AND PLECKSTRIN DOMAIN-CONTAINING PROTEIN 1; FARP1 *602655 : SOLUTE CARRIER FAMILY 4, ANION EXCHANGER, MEMBER 1, ADAPTOR PROTEIN; SLC4A1AP *602656 : ENDONUCLEASE III-LIKE 1; NTHL1 *602657 : G PROTEIN-COUPLED RECEPTOR 64; GPR64 *602658 : PHOSPHODIESTERASE 2A, cGMP-STIMULATED; PDE2A *602659 : MENAGE A TROIS 1; MNAT1 *602660 : TUBULIN, BETA-2 *602661 : TUBULIN, BETA-4 *602662 : TUBULIN, BETA-5 *602663 : PREPROPROLACTIN-RELEASING PEPTIDE *602664 : CASPASE 4, APOPTOSIS-RELATED CYSTEINE PROTEASE; CASP4 *602665 : CASPASE 5, APOPTOSIS-RELATED CYSTEINE PROTEASE; CASP5 *602666 : MYOSIN XVA; MYO15A *602667 : NIJMEGEN BREAKAGE SYNDROME GENE; NBS1 #602668 : DYSTROPHIA MYOTONICA 2; DM2 *602669 : PAIRED-LIKE HOMEODOMAIN TRANSCRIPTION FACTOR 3; PITX3 *602670 : POLYMERASE, DNA, EPSILON-2; POLE2 *602671 : GLUCOSE-6-PHOSPHATE TRANSPORTER 1; G6PT1 *602672 : RAS-ASSOCIATED PROTEIN RAB13; RAB13 *602673 : KALLIKREIN 10; KLK10 ^602674 : MOVED TO 601802 *602675 : ARGINYL AMINOPEPTIDASE; RNPEP *602676 : PHOSPHODIESTERASE 6D, cGMP-SPECIFIC, ROD, DELTA; PDE6D *602677 : RING FINGER PROTEIN 5; RNF5 *602678 : MAP/MICROTUBULE AFFINITY-REGULATING KINASE 3; MARK3 *602679 : PHOSPHATE CYTIDYLYLTRANSFERASE 2, ETHANOLAMINE; PCYT2 *602680 : GTPase-ACTIVATING PROTEIN, RHO, 5; ARHGAP5 *602681 : FORKHEAD IN RHABDOMYOSARCOMA-LIKE 1; FOXO3A *602682 : BRAIN-SPECIFIC ANGIOGENESIS INHIBITOR 1; BAI1 *602683 : BRAIN-SPECIFIC ANGIOGENESIS INHIBITOR 2; BAI2 *602684 : BRAIN-SPECIFIC ANGIOGENESIS INHIBITOR 3; BAI3 *602685 : MENTAL RETARDATION, SEVERE, WITH SPASTICITY AND PIGMENTARY TAPETORETINAL DEGENERATION *602686 : MITOTIC ARREST-DEFICIENT 1, YEAST, HOMOLOG-LIKE 1; MAD1L1 *602687 : SERINE/THREONINE PROTEIN KINASE 6; STK6 *602688 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN A/B; HNRPAB *602689 : SINGED, DROSOPHILA, HOMOLOG-LIKE; SNL *602690 : SUCCINATE DEHYDROGENASE COMPLEX, SUBUNIT D, INTEGRAL MEMBRANE PROTEIN; SDHD *602691 : NUCLEAR RECEPTOR COACTIVATOR 1; NCOA1 *602692 : GLIOMA PATHOGENESIS-RELATED PROTEIN *602693 : MINICHROMOSOME MAINTENANCE, S. CEREVISIAE, HOMOLOG OF, 3; MCM3 *602694 : NADH-UBIQUINONE OXIDOREDUCTASE Fe-S PROTEIN 4; NDUFS4 *602695 : TUMOR NECROSIS FACTOR LIGAND SUPERFAMILY, MEMBER 12; TNFSF12 *602696 : MINICHROMOSOME MAINTENANCE, S. CEREVISIAE, HOMOLOG OF, 5; MCM5 *602697 : PURINERGIC RECEPTOR P2Y, G PROTEIN-COUPLED, 11; P2RY11 *602698 : NUCLEAR FACTOR OF ACTIVATED T CELLS, CYTOPLASMIC, CALCINEURIN-DEPENDENT 3; NFATC3 *602699 : NUCLEAR FACTOR OF ACTIVATED T CELLS, CYTOPLASMIC, CALCINEURIN-DEPENDENT 4; NFATC4 *602700 : E1A-BINDING PROTEIN, 300-KD; EP300 *602701 : SARCOLEMMAL-ASSOCIATED PROTEIN *602702 : MANNOSE 6-PHOSPHATE RECEPTOR-BINDING PROTEIN, 47-KD *602703 : KATANIN, p80 SUBUNIT, B1; KATNB1 *602704 : MOUSE DOUBLE MINUTE 4 HOMOLOG; MDM4 *602705 : SYNAPSIN III; SYN3 *602706 : PROTEASOME 26S SUBUNIT, ATPase, 1; PSMC1 *602707 : PROTEASOME 26S SUBUNIT, ATPase, 4; PSMC4 *602708 : PROTEASOME 26S SUBUNIT, ATPase, 6; PSMC6 *602709 : AMYLOID BETA A4 PRECURSOR PROTEIN-BINDING, FAMILY B, MEMBER 1; APBB1 *602710 : AMYLOID BETA A4 PRECURSOR PROTEIN-BINDING, FAMILY B, MEMBER 2; APBB2 *602711 : FE65-LIKE 2 *602712 : AMYLOID BETA A4 PRECURSOR PROTEIN-BINDING, FAMILY A, MEMBER 2; APBA2 *602713 : A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 9; ADAM9 *602714 : A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 12; ADAM12 *602715 : LEIOMODIN 1; LMOD1 *602716 : NEPHRIN *602717 : GLUTAMATE RECEPTOR, IONOTROPIC, N-METHYL-D-ASPARTATE, SUBUNIT 2D; GRIN2D *602718 : TRANSFORMER 2, DROSOPHILA, HOMOLOG OF, ALPHA *602719 : SPLICING FACTOR, ARGININE/SERINE-RICH, 10; SFRS10 *602720 : PARAOXONASE 3; PON3 *602721 : DISRUPTED MEIOTIC cDNA 1, YEAST, HOMOLOG OF; DMC1 #602722 : RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR *602723 : PSORIASIS SUSCEPTIBILITY 2; PSORS2 *602724 : PEANUT-LIKE 1; PNUTL1 *602725 : INTERFERON-RELATED DEVELOPMENTAL REGULATOR 2; IFRD2 *602726 : CHLORIDE CHANNEL 6; CLCN6 *602727 : CHLORIDE CHANNEL 7; CLCN7 *602728 : MACROPHAGE SCAVENGER RECEPTOR-LIKE 1 *602729 : GAMMA-AMINOBUTYRIC ACID RECEPTOR, PI; GABRP *602730 : ACTIVIN A RECEPTOR, TYPE IIB; ACVR2B *602731 : FYN-BINDING PROTEIN; FYB *602732 : GTPase-ACTIVATING PROTEIN, RHO, 1; ARHGAP1 *602733 : ALDEHYDE DEHYDROGENASE, FAMILY 9, SUBFAMILY A, MEMBER 1; ALDH9A1 *602734 : PLASTIN 1; PLS1 *602735 : RETICULOCALBIN 1; RCN1 *602736 : ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL F0 COMPLEX, SUBUNIT C, ISOFORM 3; ATP5G3 *602737 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A (CYS-CYS), MEMBER 21; SCYA21 *602738 : KARYOPHERIN BETA-1; KPNB1 *602739 : PROTEIN KINASE, AMP-ACTIVATED, CATALYTIC, ALPHA-1; PRKAA1 *602740 : PROTEIN KINASE, AMP-ACTIVATED, NONCATALYTIC, BETA-1; PRKAB1 *602741 : PROTEIN KINASE, AMP-ACTIVATED, NONCATALYTIC, BETA-2; PRKAB2 *602742 : PROTEIN KINASE, AMP-ACTIVATED, NONCATALYTIC, GAMMA-1; PRKAG1 *602743 : PROTEIN KINASE, AMP-ACTIVATED, NONCATALYTIC, GAMMA-2; PRKAG2 *602744 : GLYCERONEPHOSPHATE O-ACYLTRANSFERASE; GNPAT *602745 : PHOSPHATIDYLINOSITOL-4-PHOSPHATE 5-KINASE, TYPE I, BETA; PIP5K1B *602746 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 14; TNFRSF14 *602747 : DUAL-SPECIFICITY PHOSPHATASE 4; DUSP4 *602748 : DUAL-SPECIFICITY PHOSPHATASE 6; DUSP6 *602749 : DUAL-SPECIFICITY PHOSPHATASE 7; DUSP7 *602750 : D-DOPACHROME TAUTOMERASE; DDT *602751 : BTB AND CNC HOMOLOGY 1; BACH1 *602752 : RAN-BINDING PROTEIN 2-LIKE 1; RANBP2L1 *602753 : ARISTALESS HOMEO BOX, DROSOPHILA, HOMOLOG OF; ARIX *602754 : POTASSIUM CHANNEL, CALCIUM-ACTIVATED, INTERMEDIATE/SMALL CONDUCTANCE, SUBFAMILY N, MEMBER 4; KCNN4 602755 : CYCLIN B2; CCNB2 *602756 : EPHRIN A2; EFNA2 *602757 : EPHRIN RECEPTOR EphB6; EPHB6 *602758 : PHOSPHATIDYLINOSITOL 4-KINASE, CATALYTIC, BETA; PIK4CB *602759 : PREDISPOSING FOR PROSTATE CANCER; PCAP *602760 : KERATIN, HAIR, ACIDIC, 2; KRTHA2 *602761 : KERATIN, HAIR, ACIDIC, 3A; KRTHA3A *602762 : KERATIN, HAIR, ACIDIC, 3B; KRTHA3B *602763 : KERATIN, HAIR, ACIDIC, 4; KRTHA4 *602764 : KERATIN, HAIR, ACIDIC, 5; KRTHA5 *602765 : KERATIN, HAIR, BASIC, 3; KRTHB3 *602766 : KERATIN, HAIR, BASIC, 4; KRTHB4 *602767 : KERATIN, HAIR, BASIC, 5; KRTHB5 *602768 : DELTA-LIKE 3; DLL3 *602769 : DNA METHYLTRANSFERASE 3A; DNMT3A *602770 : CHROMOBOX HOMOLOG 2, DROSOPHILA POLYCOMB CLASS; CBX2 #602771 : RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1 *602772 : RETINITIS PIGMENTOSA 25; RP25 *602773 : RENAL CELL CARCINOMA 4 *602774 : RAD51, S. CEREVISIAE, HOMOLOG OF, C; RAD51C *602775 : SUPPRESSOR OF CLEAR, C. ELEGANS, HOMOLOG OF; SHOC2 *602776 : REV3, S. CEREVISIAE, HOMOLOG-LIKE; REV3L *602777 : SMALL NUCLEAR RNA-ACTIVATING PROTEIN COMPLEX, POLYPEPTIDE 4; SNAPC4 *602778 : NUCLEAR RECEPTOR SUBFAMILY 6, GROUP A, MEMBER 1; NR6A1 *602779 : COAGULATION FACTOR II RECEPTOR-LIKE 3; F2RL3 *602780 : HYPERPOLARIZATION-ACTIVATED CYCLIC NUCLEOTIDE-GATED POTASSIUM CHANNEL 1; HCN1 *602781 : HYPERPOLARIZATION-ACTIVATED CYCLIC NUCLEOTIDE-GATED POTASSIUM CHANNEL 2; HCN2 *602782 : HISTIOCYTOSIS WITH JOINT CONTRACTURES AND SENSORINEURAL DEAFNESS *602783 : SPASTIC PARAPLEGIA 7 GENE; SPG7 *602784 : CORTISTATIN; CORT *602785 : H1 HISTONE FAMILY, MEMBER X; H1FX *602786 : H2A HISTONE FAMILY, MEMBER A; H2AFA *602787 : H2A HISTONE FAMILY, MEMBER C; H2AFC *602788 : H2A HISTONE FAMILY, MEMBER D; H2AFD ^602789 : MOVED TO 300163 *602790 : FOUR-AND-A-HALF LIM DOMAINS 3; FHL3 *602791 : H2A HISTONE FAMILY, MEMBER E; H2AFE *602792 : H2A HISTONE FAMILY, MEMBER G; H2AFG *602793 : H2A HISTONE FAMILY, MEMBER I; H2AFI *602794 : H2A HISTONE FAMILY, MEMBER L; H2AFL *602795 : H2A HISTONE FAMILY, MEMBER M; H2AFM *602796 : H2A HISTONE FAMILY, MEMBER N; H2AFN *602797 : H2A HISTONE FAMILY, MEMBER Q; H2AFQ *602798 : H2B HISTONE FAMILY, MEMBER A; H2BFA *602799 : H2B HISTONE FAMILY, MEMBER B; H2BFB *602800 : H2B HISTONE FAMILY, MEMBER C; H2BFC *602801 : H2B HISTONE FAMILY, MEMBER D; H2BFD *602802 : H2B HISTONE FAMILY, MEMBER E; H2BFE *602803 : H2B HISTONE FAMILY, MEMBER F; H2BFF *602804 : H2B HISTONE FAMILY, MEMBER G; H2BFG *602805 : H2B HISTONE FAMILY, MEMBER H; H2BFH *602806 : H2B HISTONE FAMILY, MEMBER J; H2BFJ *602807 : H2B HISTONE FAMILY, MEMBER K; H2BFK *602808 : H2B HISTONE FAMILY, MEMBER N; H2BFN *602809 : KINESIN FAMILY MEMBER 5B; KIF5B *602810 : H3 HISTONE FAMILY, MEMBER A; H3FA *602811 : H3 HISTONE FAMILY, MEMBER B; H3FB *602812 : H3 HISTONE FAMILY, MEMBER C; H3FC *602813 : H3 HISTONE FAMILY, MEMBER D; H3FD *602814 : H3 HISTONE FAMILY, MEMBER F; H3FF *602815 : H3 HISTONE FAMILY, MEMBER H; H3FH *602816 : H3 HISTONE FAMILY, MEMBER I; H3FI *602817 : H3 HISTONE FAMILY, MEMBER J; H3FJ *602818 : H3 HISTONE FAMILY, MEMBER K; H3FK *602819 : H3 HISTONE FAMILY, MEMBER L; H3FL *602820 : H3 HISTONE FAMILY, MEMBER T; H3FT *602821 : KINESIN FAMILY MEMBER 5A; KIF5A *602822 : H4 HISTONE FAMILY, MEMBER A; H4FA *602823 : H4 HISTONE FAMILY, MEMBER B; H4FB *602824 : H4 HISTONE FAMILY, MEMBER C; H4FC *602825 : H4 HISTONE FAMILY, MEMBER D; H4FD *602826 : H4 HISTONE FAMILY, MEMBER E; H4FE *602827 : H4 HISTONE FAMILY, MEMBER G; H4FG *602828 : H4 HISTONE FAMILY, MEMBER H; H4FH *602829 : H4 HISTONE FAMILY, MEMBER I; H4FI *602830 : H4 HISTONE FAMILY, MEMBER J; H4FJ *602831 : H4 HISTONE FAMILY, MEMBER K; H4FK *602832 : H4 HISTONE FAMILY, MEMBER L; H4FL *602833 : H4 HISTONE FAMILY, MEMBER M; H4FM ^602834 : MOVED TO 600279 *602835 : GROWTH ARREST-SPECIFIC 2; GAS2 *602836 : PURINERGIC RECEPTOR P2X, LIGAND-GATED ION CHANNEL, 5; P2RX5 *602837 : DNAJ, E. COLI, HOMOLOG OF, SUBFAMILY A, MEMBER 1; DNAJA1 *602838 : PHOSPHATIDYLINOSITOL 3-KINASE, CLASS 2, BETA; PIK3C2B *602839 : PHOSPHATIDYLINOSITOL 3-KINASE, CATALYTIC, DELTA; PIK3CD *602840 : TUMOR NECROSIS FACTOR LIGAND SUPERFAMILY, MEMBER 7; TNFSF7 *602841 : ALDEHYDE OXIDASE 1; AOX1 *602842 : GEMININ *602843 : RHO GDP-DISSOCIATION INHIBITOR BETA; ARHGDIB *602844 : RHO GDP-DISSOCIATION INHIBITOR GAMMA; ARHGDIG *602845 : KINESIN FAMILY MEMBER 3C; KIF3C *602846 : HUNTINGTIN-INTERACTING PROTEIN 2; HIP2 *602847 : H2B HISTONE FAMILY, MEMBER L; H2BFL *602848 : SKELETAL MUSCLE ABUNDANT PROTEIN #602849 : MUENKE SYNDROME *602850 : RING FINGER PROTEIN 4; RNF4 *602851 : VERY LARGE G PROTEIN-COUPLED RECEPTOR 1 *602852 : NUCLEOSIDE DIPHOSPHATE-LINKED MOIETY X MOTIF, 2; NUDT2 *602853 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, R; PTPRR *602854 : PROTEASOME SUBUNIT, ALPHA-TYPE, 1; PSMA1 *602855 : PROTEASOME SUBUNIT, ALPHA-TYPE, 6; PSMA6 *602856 : REGULATOR OF G PROTEIN SIGNALING 10; RGS10 *602857 : CHIMERIN 2; CHN2 *602858 : 7-@DEHYDROCHOLESTEROL REDUCTASE; DHCR7 *602859 : PEROXISOME BIOGENESIS FACTOR 10; PEX10 *602860 : BUDDING UNINHIBITED BY BENZIMIDAZOLES 1, S. CEREVISIAE, HOMOLOG OF, BETA; BUB1B *602861 : PLAKOPHILIN 2; PKP2 *602862 : UDP-N-ACETYLGLUCOSAMINE PYROPHOSPHORYLASE 1; UAP1 *602863 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 14; WNT14 *602864 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 15; WNT15 *602865 : DELETED IN BLADDER CANCER CHROMOSOME REGION CANDIDATE 1; DBCCR1 *602866 : CATION CHANNEL, AMILORIDE-SENSITIVE, NEURONAL, 2; ACCN2 *602867 : INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN 7; IGFBP7 *602868 : CELL DIVISION CYCLE 5, S. POMBE, HOMOLOG-LIKE; CDC5L *602869 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN U; HNRPU *602870 : INTERPHOTORECEPTOR MATRIX PROTEOGLYCAN 1; IMPG1 *602871 : PERIPLAKIN; PPL *602872 : CHLORIDE INTRACELLULAR CHANNEL 1; CLIC1 *602873 : NEBULIN-RELATED ANCHORING PROTEIN; NRAP *602874 : UDP-GLUCOSE CERAMIDE GLUCOSYLTRANSFERASE; UGCG *602875 : ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDM *602876 : OCCLUDIN; OCLN *602877 : PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 7; PPP1R7 *602878 : SOLUTE CARRIER FAMILY 30, MEMBER 3; SLC30A3 *602879 : ERYTHROCYTE MEMBRANE PROTEIN BAND 4.1-LIKE 1; EPB41L1 *602880 : GROWTH/DIFFERENTIATION FACTOR 1; GDF1 *602881 : PHD FINGER PROTEIN 1; PHF1 *602882 : LEUKOCYTE CELL-DERIVED CHEMOTAXIN 2; LECT2 *602883 : SOLUTE CARRIER FAMILY 21, MEMBER 3; SLC21A3 *602884 : GDP-MANNOSE 4,6-DEHYDRATASE; GMDS *602885 : G PROTEIN-COUPLED RECEPTOR 38; GPR38 *602886 : G PROTEIN-COUPLED RECEPTOR 39; GPR39 *602887 : DISCS LARGE, DROSOPHILA, HOMOLOG OF, 4; DLG4 *602888 : BETAINE-HOMOCYSTEINE METHYLTRANSFERASE; BHMT *602889 : A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 3A; ADAM3A *602890 : KILLER CELL LECTIN-LIKE RECEPTOR, SUBFAMILY B, MEMBER 1; KLRB1 *602891 : KILLER CELL LECTIN-LIKE RECEPTOR, SUBFAMILY C, MEMBER 2; KLRC2 *602892 : KILLER CELL LECTIN-LIKE RECEPTOR, SUBFAMILY C, MEMBER 3; KLRC3 *602893 : KILLER CELL LECTIN-LIKE RECEPTOR, SUBFAMILY C, MEMBER 4; KLRC4 *602894 : KILLER CELL LECTIN-LIKE RECEPTOR, SUBFAMILY D, MEMBER 1; KLRD1 *602895 : SCAFFOLD ATTACHMENT FACTOR B; SAFB *602896 : MITOGEN-ACTIVATED PROTEIN KINASE 9; MAPK9 *602897 : MITOGEN-ACTIVATED PROTEIN KINASE 10; MAPK10 *602898 : MITOGEN-ACTIVATED PROTEIN KINASE 11; MAPK11 *602899 : MITOGEN-ACTIVATED PROTEIN KINASE 13; MAPK13 *602900 : DNA METHYLTRANSFERASE 3B; DNMT3B *602901 : KARYOPHERIN BETA-2; KPNB2 *602902 : BASIC TRANSCRIPTION ELEMENT-BINDING PROTEIN 1; BTEB1 *602903 : KRUPPEL-LIKE FACTOR 5; KLF5 *602904 : MITOGEN-ACTIVATED PROTEIN KINASE 6; MAPK6 *602905 : POTASSIUM CHANNEL, VOLTAGE-GATED, DELAYED-RECTIFIER, SUBFAMILY S, MEMBER 1; KCNS1 *602906 : POTASSIUM CHANNEL, VOLTAGE-GATED, DELAYED-RECTIFIER, SUBFAMILY S, MEMBER 2; KCNS2 *602907 : CENTRIN 3; CETN3 *602908 : RETINOMA-BINDING PROTEIN 9; RBBP9 *602909 : CLAUDIN 4; CLDN4 *602910 : CLAUDIN 3; CLDN3 *602911 : CALCIUM CHANNEL, VOLTAGE-DEPENDENT, GAMMA-2 SUBUNIT; CACNG2 *602912 : INTEGRIN, BETA-4, BINDING PROTEIN OF; ITGB4BP *602913 : CYTOKINE-INDUCIBLE KINASE; CNK *602914 : AQUAPORIN 9; AQP9 *602915 : TRYPTOPHAN-RICH BASIC PROTEIN; WRB *602916 : UBIQUITIN-CONJUGATING ENZYME E2E 1; UBE2E1 *602917 : DOWN SYNDROME CRITICAL REGION GENE 1; DSCR1 *602918 : PHENYLALANINE-tRNA SYNTHETASE-LIKE; FARSL *602919 : DOCKING PROTEIN 1; DOK1 *602920 : LIM AND SH3 PROTEIN 1; LASP1 *602921 : PERSEPHIN; PSPN *602922 : RETINOBLASTOMA-BINDING PROTEIN 7; RBBP7 *602923 : RETINOBLASTOMA-BINDING PROTEIN 4; RBBP4 *602924 : RAS HOMOLOG GENE FAMILY, MEMBER E; ARHE *602925 : PHOSPHATIDYLINOSITOL 3-KINASE, CATALYTIC, BETA; PIK3CB *602926 : SYNTAXIN-BINDING PROTEIN 1; STXBP1 *602927 : G PROTEIN-COUPLED RECEPTOR 19; GPR19 *602928 : TROPOMODULIN 2; TMOD2 *602929 : LOSS OF HETEROZYGOSITY, 11, CHROMOSOMAL REGION 2, GENE A; LOH11CR2A *602930 : PREVENTS MITOTIC CATASTROPHE 2, XENOPUS, HOMOLOG OF; XPMC2H *602931 : MOTHERS AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 6; MADH6 *602932 : MOTHERS AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 7; MADH7 *602933 : THYROID HORMONE RECEPTOR INTERACTOR 6; TRIP6 *602934 : STROMAL CELL-DERIVED FACTOR 2; SDF2 *602935 : FATTY ACID AMIDE HYDROLASE; FAAH ^602936 : MOVED TO 300149 *602937 : CBP/p300-INTERACTING TRANSACTIVATOR, WITH GLU/ASP-RICH C-TERMINAL DOMAIN, 2; CITED2 *602938 : BILE ACID CoA:AMINO ACID N-ACYLTRANSFERASE; BAAT *602939 : FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 18; FKHL18 *602940 : MARCKS-LIKE PROTEIN; MLP *602941 : BREAST CANCER ANTIESTROGEN RESISTANCE 1; BCAR1 *602942 : NEUROBLASTOMA STAGE 4S GENE *602943 : RAR-RELATED ORPHAN RECEPTOR C; RORC *602944 : E2F TRANSCRIPTION FACTOR 6; E2F6 *602945 : TRANSCRIPTIONAL ADAPTOR 3-LIKE *602946 : TAF6-LIKE RNA POLYMERASE II; TAF6L *602947 : SUPPRESSOR OF TY 3, S. CEREVISIAE, HOMOLOG OF; SUPT3H *602948 : RAD51, S. CEREVISIAE, HOMOLOG OF, B; RAD51L1 *602949 : SIN3-ASSOCIATED POLYPEPTIDE, 18-KD; SAP18 *602950 : HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN METHYLTRANSFERASE 1-LIKE 2; HRMT1L2 *602951 : ZINC FINGER PROTEIN 37, MOUSE, HOMOLOG OF; ZFP37 *602952 : WOLF-HIRSCHHORN SYNDROME CANDIDATE 1; WHSC1 *602953 : HAIRY/ENHANCER OF SPLIT-RELATED WITH YRPW MOTIF 1; HEY1 *602954 : RAD51, S. CEREVISIAE, HOMOLOG OF, D; RAD51L3 *602955 : TAF6 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 80-KD; TAF6 *602956 : X-RAY REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 9; XRCC9 *602957 : SMALL INDUCIBLE CYTOKINE SUBFAMILY A, MEMBER 22; SCYA22 *602958 : SERUM/GLUCOCORTICOID-REGULATED KINASE; SGK *602959 : EUKARYOTIC TRANSLATION ELONGATION FACTOR 1, ALPHA-2; EEF1A2 *602960 : DELTA SLEEP-INDUCING PEPTIDE, IMMUNOREACTOR; DSIPI *602961 : UBIQUITIN-CONJUGATING ENZYME E2D 1; UBE2D1 *602962 : UBIQUITIN-CONJUGATING ENZYME E2D 2; UBE2D2 *602963 : UBIQUITIN-CONJUGATING ENZYME E2D 3; UBE2D3 *602964 : TRANSLIN-ASSOCIATED FACTOR X; TSNAX *602965 : FATTY ACID-BINDING PROTEIN 7; FABP7 *602966 : OROFACIAL CLEFT 2; OFC2 *602967 : ZINC FINGER PROTEIN 217; ZNF217 *602968 : BREAST CARCINOMA AMPLIFIED SEQUENCE 1; BCAS1 *602969 : ESTROGEN-RELATED RECEPTOR, GAMMA; ESRRG *602970 : KARYOPHERIN ALPHA-4; KPNA4 *602971 : TUBULIN-SPECIFIC CHAPERONE C; TBCC *602972 : PHOSPHODIESTERASE 8A; PDE8A *602973 : PHOSPHODIESTERASE 9A; PDE9A *602974 : AQUAPORIN 7; AQP7 602975 : TELOMERE LENGTH REGULATOR *602976 : MAX-LIKE PROTEIN X; MLX *602977 : GLYCOPROTEIN 2, ZYMOGEN GRANULE MEMBRANE; GP2 *602978 : EARLY DEVELOPMENT REGULATOR 1; EDR1 *602979 : EARLY DEVELOPMENT REGULATOR 2; EDR2 *602980 : PROTEIN KINASE, SERINE/ARGININE-SPECIFIC, 2; SRPK2 *602981 : AE-BINDING PROTEIN 1; AEBP1 *602982 : POTASSIUM CHANNEL, CALCIUM-ACTIVATED, INTERMEDIATE/SMALL CONDUCTANCE, SUBFAMILY N, MEMBER 1; KCNN1 *602983 : POTASSIUM CHANNEL, CALCIUM-ACTIVATED, INTERMEDIATE/SMALL CONDUCTANCE, SUBFAMILY N, MEMBER 3; KCNN3 *602984 : RNA POLYMERASE II TRANSCRIPTIONAL REGULATION MEDIATOR *602985 : NADH-UBIQUINONE OXIDOREDUCTASE Fe-S PROTEIN 2; NDUFS2 *602986 : DEVELOPMENTALLY REGULATED GTP-BINDING PROTEIN 2; DRG2 *602987 : PHOSPHODIESTERASE 1C; PDE1C *602988 : PROTOCADHERIN 7; PCDH7 *602989 : CDC-LIKE KINASE 2; CLK2 *602990 : CDC-LIKE KINASE 3; CLK3 *602991 : NOGGIN, MOUSE, HOMOLOG OF; NOG *602992 : LEUKOCYTE-ASSOCIATED IMMUNOGLOBULIN-LIKE RECEPTOR 1; LAIR1 *602993 : LEUKOCYTE-ASSOCIATED IMMUNOGLOBULIN-LIKE RECEPTOR 2; LAIR2 *602994 : LEUKOREGULIN *602995 : UBIQUITIN-CONJUGATING ENZYME E2 VARIANT 1; UBE2V1 *602996 : IMMEDIATE-EARLY RESPONSE 3; IER3 *602997 : CUBILIN; CUBN *602998 : SYNUCLEIN, GAMMA; SNCG *602999 : PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 3C; PPP1R3C *603000 : IMMATURE COLON CARCINOMA TRANSCRIPT 1; ICT1 *603001 : UBIQUITIN-CONJUGATING ENZYME E2 VARIANT 2; UBE2V2 *603002 : TRANSPORTIN 2 603003 : BILE DUCT CYSTS *603004 : GLIOBLASTOMA AMPLIFIED SEQUENCE; GBAS *603005 : 3-PRIME-@PHOSPHOADENOSINE 5-PRIME-PHOSPHOSULFATE SYNTHASE 2; PAPSS2 *603006 : CADHERIN 4; CDH4 *603007 : CADHERIN 6; CDH6 *603008 : CADHERIN 8; CDH8 *603009 : DYSFERLIN; DYSF *603010 : DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 17; DFNB17 *603011 : SMALL EDRK-RICH FACTOR 1A; SERF1A *603012 : HEAT-SHOCK 70-KD PROTEIN 1B; HSPA1B 603013 : SCHIZOPHRENIA 6; SCZD6 *603014 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE 7; MAP2K7 *603015 : TRANSFORMATION/TRANSCRIPTION DOMAIN-ASSOCIATED PROTEIN; TRRAP *603016 : CADHERIN 19; CDH19 *603017 : CADHERIN 17; CDH17 *603018 : UDP-GAL:BETA-GlcNAc BETA-1,3-GALACTOSYLTRANSFERASE, POLYPEPTIDE 2; B3GALT2 *603019 : CADHERIN 18; CDH18 *603020 : ATPase FAMILY GENE 3-LIKE 1; AFG3L1 *603021 : MITOCHONDRIAL RIBOSOMAL PROTEIN S12; MRPS12 *603022 : E4F TRANSCRIPTION FACTOR 1; E4F1 *603023 : ZINC FINGER PROTEIN, SUBFAMILY 1A, MEMBER 1; ZNFN1A1 *603024 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY F, MEMBER 1; SMARCF1 *603025 : PHOSPHATIDYLINOSITOL-BINDING CLATHRIN ASSEMBLY PROTEIN; PICALM *603026 : PLEOMORPHIC ADENOMA GENE 1; PLAG1 *603027 : FRUCTOSE-1,6-BISPHOSPHATASE 2; FBP2 *603028 : TOLL-LIKE RECEPTOR 2; TLR2 *603029 : TOLL-LIKE RECEPTOR 3; TLR3 *603030 : TOLL-LIKE RECEPTOR 4; TLR4 *603031 : TOLL-LIKE RECEPTOR 5; TLR5 *603032 : STANNIN; SNN *603033 : COLLAGENIC TAIL OF ENDPLATE ACETYLCHOLINESTERASE; COLQ #603034 : ENDPLATE ACETYLCHOLINESTERASE DEFICIENCY; EAD *603035 : INTERLEUKIN 16; IL16 ^603036 : MOVED TO 601877 *603037 : LEFT-RIGHT DETERMINATION, FACTOR B; LEFTB *603038 : SPERM-ASSOCIATED ANTIGEN 4; SPAG4 *603039 : MAX-BINDING PROTEIN; MNT *603040 : TUMOR SUPPRESSOR GENE ON CHROMOSOME 11 #603041 : MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME; MNGIE *603042 : SMT3, YEAST, HOMOLOG 2; SMT3H2 *603043 : NEUTRAL SPHINGOMYELINASE ACTIVATION-ASSOCIATED FACTOR; NSMAF *603044 : PLEOMORPHIC ADENOMA GENE-LIKE 1; PLAGL1 *603045 : LOSS OF HETEROZYGOSITY, 18, CHROMOSOMAL REGION 1; LOH18CR1 *603046 : TRANSLOCATION IN RENAL CARCINOMA ON CHROMOSOME 8 *603047 : ASTIGMATISM *603048 : GLYCOSYLPHOSPHATIDYLINOSITOL ANCHOR ATTACHMENT PROTEIN 1; GPAA1 *603049 : THIOREDOXIN-LIKE; TXNL *603050 : SPECTRIN SH3 DOMAIN-BINDING PROTEIN 1; SSH3BP1 *603051 : ALKYLGLYCERONE-PHOSPHATE SYNTHASE; AGPS *603052 : CLEAVAGE AND POLYADENYLATION SPECIFICITY FACTOR 4; CPSF4 *603053 : HISTONE ACETYLTRANSFERASE 1; HAT1 *603054 : CYSTEINE KNOT SUPERFAMILY 1, BMP ANTAGONIST 1; CKTSF1B1 *603055 : SKI-INTERACTING PROTEIN *603056 : ORIGIN RECOGNITION COMPLEX, SUBUNIT 4, S. CEREVISIAE, HOMOLOG OF; ORC4L *603057 : PROTOCADHERIN 16; PCDH16 *603058 : PROTOCADHERIN-GAMMA, SUBFAMILY B, MEMBER 4; PCDHGB4 *603059 : PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 12; PCDHGA12 *603060 : KINESIN FAMILY MEMBER 1C; KIF1C *603061 : ENDOSULFINE, ALPHA; ENSA *603062 : TRANS-GOLGI NETWORK PROTEIN, 46-KD *603063 : 3-@HYDROXYBUTYRATE DEHYDROGENASE; BDH *603064 : URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASE 2 FAMILY, MEMBER B11; UGT2B11 *603065 : NUCLEAR RECEPTOR SUBFAMILY 1, GROUP I, MEMBER 2; NR1I2 *603066 : PROCOLLAGEN-LYSINE, 2-OXOGLUTARATE 5-DIOXYGENASE 3; PLOD3 ^603067 : MOVED TO 602413 *603068 : DUAL-SPECIFICITY PHOSPHATASE 2; DUSP2 *603069 : DUAL-SPECIFICITY PHOSPHATASE 5; DUSP5 *603070 : RAD51-INTERACTING PROTEIN *603071 : G PROTEIN-COUPLED RECEPTOR 17; GPR17 *603072 : SERINE/THREONINE PROTEIN KINASE 15; STK15 *603073 : ZINC FINGER PROTEIN OF CEREBELLUM, 2; ZIC2 *603074 : PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE, ISOFORM 1B, GAMMA SUBUNIT; PAFAH1B3 *603075 : MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1 *603076 : ATP-BINDING CASSETTE, SUBFAMILY G, MEMBER 1; ABCG1 ^603077 : MOVED TO 300157 *603078 : CHECKPOINT, S. POMBE, HOMOLOG OF, 1; CHEK1 *603079 : CHROMOBOX HOMOLOG 4, DROSOPHILA POLYCOMB CLASS; CBX4 *603080 : SOLUTE CARRIER FAMILY 6, MEMBER 12; SLC6A12 *603081 : ADP-RIBOSYLARGININE HYDROLASE; ADPRH ^603082 : MOVED TO 188855 *603083 : HETEROGENEOUS NUCLEAR RIBOPROTEIN L; HNRPL *603084 : ASPARTYL-tRNA SYNTHETASE; DARS *603085 : SOLUTE CARRIER FAMILY 31 (COPPER TRANSPORTER), MEMBER 1; SLC31A1 *603086 : ADP-RIBOSYLTRANSFERASE 3; ART3 *603087 : ADP-RIBOSYLTRANSFERASE 4; ART4 *603088 : SOLUTE CARRIER FAMILY 31 (COPPER TRANSPORTER), MEMBER 2; SLC31A2 *603089 : BRCA1-ASSOCIATED PROTEIN 1; BAP1 *603090 : UBIQUITIN CARBOXYL-TERMINAL ESTERASE L3; UCHL3 *603091 : UBIQUITIN-SPECIFIC PROTEASE 12; USP12 *603092 : DUAL-SPECIFICITY PHOSPHATASE 11; DUSP11 *603093 : UDP-GAL:BETA-GlcNAc BETA-1,3-GALACTOSYLTRANSFERASE, POLYPEPTIDE 1; B3GALT1 *603094 : UDP-GAL:BETA-GlcNAc BETA-1,3-GALACTOSYLTRANSFERASE, POLYPEPTIDE 3; B3GALT3 *603095 : UDP-GAL:BETA-GlcNAc BETA-1,3-GALACTOSYLTRANSFERASE, POLYPEPTIDE 4; B3GALT4 *603096 : ACHROMATOPSIA 1; ACHM1 *603097 : ATPase, H+ TRANSPORTING, LYSOSOMAL, 42-KD, V1 SUBUNIT C, ISOFORM 1; ATP6V1C1 *603098 : DEAFNESS, AUTOSOMAL RECESSIVE 13; DFNB13 *603099 : 1-@ACYLGLYCEROL-3-PHOSPHATE O-ACYLTRANSFERASE 1; AGPAT1 *603100 : 1-@ACYLGLYCEROL-3-PHOSPHATE O-ACYLTRANSFERASE 2; AGPAT2 *603101 : CARBOXYPEPTIDASE B2, PLASMA; CPB2 *603102 : CARBOXYPEPTIDASE D; CPD *603103 : CARBOXYPEPTIDASE N, POLYPEPTIDE 1, 50-KD; CPN1 *603104 : CARBOXYPEPTIDASE N, POLYPEPTIDE 2, 83-KD; CPN2 *603105 : CARBOXYPEPTIDASE Z; CPZ *603106 : NEURONATIN; NNAT *603107 : TRANSCRIPTION FACTOR 20; TCF20 *603108 : MICROTUBULE-ASSOCIATED PROTEIN, RP/EB FAMILY, MEMBER 1; MAPRE1 *603109 : MOTHERS AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 3; MADH3 *603110 : MOTHERS AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 5; MADH5 *603111 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY E, MEMBER 1; SMARCE1 *603112 : S100 CALCIUM-BINDING PROTEIN A12; S100A12 *603113 : PROTEIN PHOSPHATASE 2, STRUCTURAL/REGULATORY SUBUNIT A, BETA; PPP2R1B *603114 : S100 CALCIUM-BINDING PROTEIN A11; S100A11 *603115 : DEAD/H BOX 9; DDX9 603116 : CRANIOSYNOSTOSIS, ANAL ANOMALIES, AND POROKERATOSIS 603117 : SPASTIC PARAPLEGIA, OPTIC ATROPHY, MICROCEPHALY, AND XY SEX REVERSAL *603118 : CADHERIN 16; CDH16 603119 : APRAXIA OF EYELID OPENING *603120 : QUIESCIN Q6; QSCN6 *603121 : CYLICIN 1; CYCL1 *603122 : DEDICATOR OF CYTOKINESIS 2; DOCK2 *603123 : DEDICATOR OF CYTOKINESIS 3; DOCK3 *603124 : UBIQUITIN-CONJUGATING ENZYME E2G 2; UBE2G2 *603125 : TYROSYLPROTEIN SULFOTRANSFERASE 1; TPST1 *603126 : TYROSYLPROTEIN SULFOTRANSFERASE 2; TPST2 *603127 : GROWTH ARREST-SPECIFIC 7; GAS7 *603128 : SINGLE-MINDED, DROSOPHILA, HOMOLOG OF, 1; SIM1 *603129 : LIM DOMAIN ONLY 4; LMO4 *603130 : ATTRACTIN; ATRN *603131 : PEPTIDASE-BETA, MITOCHONDRIAL PROCESSING; PMPCB *603132 : ZINC FINGER PROTEIN 189; ZNF189 603133 : DISLOCATED ELBOWS, BOWED TIBIAS, SCOLIOSIS, DEAFNESS, CATARACT, MICROCEPHALY, AND MENTAL RETARDATION *603134 : CULLIN 1; CUL1 *603135 : CULLIN 2; CUL2 *603136 : CULLIN 3; CUL3 *603137 : CULLIN 4A; CUL4A ^603138 : MOVED TO 300304 *603139 : RAD17, S. POMBE, HOMOLOG OF; RAD17 *603140 : PHOSPHATIDYLINOSITOL-4-PHOSPHATE 5-KINASE, TYPE II, ALPHA; PIP5K2A *603141 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, F POLYPEPTIDE-INTERACTING PROTEIN-BINDING PROTEIN 1; PPFIBP1 *603142 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, F POLYPEPTIDE-INTERACTING PROTEIN-BINDING PROTEIN 2; PPFIBP2 *603143 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, F POLYPEPTIDE-INTERACTING PROTEIN ALPHA-2; PPFIA2 *603144 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, F POLYPEPTIDE-INTERACTING PROTEIN ALPHA 3; PPFIA3 *603145 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, F POLYPEPTIDE-INTERACTING PROTEIN ALPHA 4; PPFIA4 *603146 : PROTEASOME 26S SUBUNIT, NON-ATPase, 9; PSMD9 #603147 : CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic *603148 : ACTIVATING TRANSCRIPTION FACTOR 3; ATF3 *603149 : INTERLEUKIN 17; IL17 *603150 : ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL F1 COMPLEX, DELTA SUBUNIT; ATP5D *603151 : CELL DIVISION CYCLE 10; CDC10 *603152 : ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL F0 COMPLEX, SUBUNIT F6; ATP5J *603153 : RAD1, S. POMBE, HOMOLOG OF; RAD1 *603154 : PININ; PNN *603155 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 14; PTPN14 *603156 : BIPHENYL HYDROLASE-LIKE; BPHL *603157 : PHOSPHATIDYLINOSITOL 3-KINASE, REGULATORY, 2; PIK3R2 *603158 : UBIQUITIN-SPECIFIC PROTEASE 8; USP8 *603159 : LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 3; LRP3 *603160 : ECTONUCLEOSIDE TRIPHOSPHATE DIPHOSPHOHYDROLASE 6; ENTPD6 *603161 : ECTONUCLEOSIDE TRIPHOSPHATE DIPHOSPHOHYDROLASE 3; ENTPD3 *603162 : ECTONUCLEOSIDE TRIPHOSPHATE DIPHOSPHOHYDROLASE 5; ENTPD5 *603163 : SCRAPIE-RESPONSIVE GENE 1 *603164 : PEROXISOME BIOGENESIS FACTOR 3; PEX3 *603165 : DERMATITIS, ATOPIC *603166 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE KINASE 2; MAP4K2 *603167 : BCL2 ANTAGONIST OF CELL DEATH; BAD *603168 : UNC51-LIKE KINASE 1; ULK1 *603169 : CATHEPSIN Z; CTSZ *603170 : TEA DOMAIN FAMILY MEMBER 3; TEAD3 *603171 : NEURAL PRECURSOR CELL EXPRESSED, DEVELOPMENTALLY DOWNREGULATED 8; NEDD8 *603172 : UBIQUITIN-ACTIVATING ENZYME E1C; UBE1C *603173 : UBIQUITIN-CONJUGATING ENZYME E2M; UBE2M #603174 : HOMOCYSTEINEMIA *603175 : SCHIZOPHRENIA 5; SCZD5 *603176 : SCHIZOPHRENIA 7; SCZD7 *603177 : VESICLE-ASSOCIATED MEMBRANE PROTEIN 8; VAMP8 *603178 : METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE; MMSDH *603179 : CARBONIC ANHYDRASE IX; CA9 *603180 : EXPORTIN, tRNA; XPOT *603181 : INTERLEUKIN ENHANCER-BINDING FACTOR 2; ILF2 *603182 : INTERLEUKIN ENHANCER-BINDING FACTOR 3; ILF3 *603183 : RETICULON 2; RTN2 *603184 : CYCLIN-DEPENDENT KINASE 8; CDK8 *603185 : NUCLEAR AUTOANTIGENIC SPERM PROTEIN; NASP *603186 : DEATH-ASSOCIATED PROTEIN 6; DAXX *603187 : CENTRIN 1; CETN1 *603188 : OBESITY, SUSCEPTIBILITY TO, ON CHROMOSOME 10; OB10 *603189 : SYNTAXIN 5A; STX5A *603190 : PROTEIN ARGININE N-METHYLTRANSFERASE 3 *603191 : CHROMOSOME 21 OPEN READING FRAME 2; C21ORF2 *603192 : ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL F0 COMPLEX, SUBUNIT C, ISOFORM 1; ATP5G1 *603193 : ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL F0 COMPLEX, SUBUNIT C, ISOFORM 2; ATP5G2 *603194 : MECKEL SYNDROME, TYPE 2; MKS2 *603195 : G PROTEIN-COUPLED RECEPTOR 32; GPR32 *603196 : COCHLIN; COCH *603197 : NEUROPATHY TARGET ESTERASE *603198 : RNA POLYMERASE I AND TRANSCRIPT RELEASE FACTOR; PTRF *603199 : INAD, DROSOPHILA, HOMOLOG OF *603200 : REGULATORY FACTOR X, ANKYRIN REPEAT-CONTAINING; RFXANK *603201 : ATP-BINDING CASSETTE, SUBFAMILY B, MEMBER 11; ABCB11 *603202 : LACTASE; LCT *603203 : CYCLIN G2; CCNG2 *603204 : EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 2 *603205 : MICRORCHIDIA, MOUSE, HOMOLOG OF 603206 : SCHIZOPHRENIA 8; SCZD8 *603207 : VTI1, S. CEREVISIAE, HOMOLOG OF *603208 : POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 13; KCNJ13 603209 : CYTIDINE MONOPHOSPHO-N-ACETYLNEURAMINIC ACID HYDROXYLASE; CMAH *603210 : JERKY, MOUSE, HOMOLOG OF; JRK *603211 : JERKY, MOUSE, HOMOLOG-LIKE; JRKL *603212 : BEADED FILAMENT STRUCTURAL PROTEIN 2; BFSP2 *603213 : KINESIN-LIKE 4; KNSL4 *603214 : ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 4; ABCD4 *603215 : N-ETHYLMALEIMIDE-SENSITIVE FACTOR ATTACHMENT PROTEIN, ALPHA; NAPA *603216 : SOLUBLE NSF-ATTACHMENT PROTEIN, GAMMA *603217 : SYNTAXIN 7; STX7 #603218 : HUNTINGTON DISEASE-LIKE 1; HDL1 *603219 : POTASSIUM CHANNEL, SUBFAMILY K, MEMBER 2; KCNK2 *603220 : POTASSIUM CHANNEL, SUBFAMILY K, MEMBER 3; KCNK3 *603221 : MYOPIA 3; MYP3 *603222 : U22 HOST GENE #603223 : RNA, U22 SMALL NUCLEOLAR; RNU22 #603224 : RNA, U25 SMALL NUCLEOLAR; RNU25 #603225 : RNA, U26 SMALL NUCLEOLAR; RNU26 #603226 : RNA, U27 SMALL NUCLEOLAR; RNU27 #603227 : RNA, U28 SMALL NUCLEOLAR; RNU28 #603228 : RNA, U29 SMALL NUCLEOLAR; RNU29 #603229 : RNA, U30 SMALL NUCLEOLAR; RNU30 #603230 : RNA, U31 SMALL NUCLEOLAR; RNU31 *603231 : ZINC FINGER PROTEIN 200; ZNF200 *603232 : OLFACTORY RECEPTOR, FAMILY 1, SUBFAMILY F, MEMBER 1; OR1F1 #603233 : PSEUDOHYPOPARATHYROIDISM, TYPE IB *603234 : ATP-BINDING CASSETTE, SUBFAMILY C, MEMBER 6; ABCC6 *603235 : SELENOPROTEIN W, 1; SEPW1 *603236 : MEVALONATE PYROPHOSPHATE DECARBOXYLASE; MVD *603237 : ERYTHROCYTE MEMBRANE PROTEIN 4.1-LIKE 2; EPB41L2 *603238 : RNA, U17D SMALL NUCLEAR; RNU17D #603239 : RNA, U17B SMALL NUCLEOLAR; RNU17B *603240 : SOLUTE CARRIER FAMILY 22 (ORGANIC CATION TRANSPORTER), MEMBER 1-LIKE-ANTISENSE; SLC22A1LS *603241 : LIMBIC SYSTEM-ASSOCIATED MEMBRANE PROTEIN; LSAMP *603242 : LECTIN, C-TYPE, SUPERFAMILY MEMBER 2; CLECSF2 *603243 : AUTOCRINE MOTILITY FACTOR RECEPTOR; AMFR *603244 : HEPARAN SULFATE D-GLUCOSAMINYL 3-O-SULFOTRANSFERASE 1; HS3ST1 *603245 : NK-2, DROSOPHILA, HOMOLOG OF, 8 *603246 : GENERAL TRANSCRIPTION FACTOR 3C, POLYPEPTIDE 1; GTF3C1 *603247 : FATTY ACID CoA LIGASE, VERY LONG-CHAIN 1; FACVL1 *603248 : BONE MORPHOGENETIC PROTEIN RECEPTOR, TYPE IB; BMPR1B *603249 : 4-@NITROPHENYLPHOSPHATASE DOMAIN AND NONNEURONAL SNAP25-LIKE 1; NIPSNAP1 *603250 : FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 6; FKHL6 *603251 : CYCLIN-DEPENDENT KINASE 9; CDK9 *603252 : FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 11; FOXL1 *603253 : CYSTATIN 7; CST7 *603254 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY A, MEMBER 4; SMARCA4 *603255 : NUCLEAR TRANSCRIPTION FACTOR, X BOX-BINDING, 1; NFX1 *603256 : LEUCINE-RICH REPEAT IN FLII-INTERACTING PROTEIN 1; LRRFIP1 *603257 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY A, MEMBER 3; SMARCA3 *603258 : INHIBITOR OF KAPPA LIGHT CHAIN GENE ENHANCER IN B CELLS, KINASE OF, BETA; IKBKB *603259 : MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 8; MAP3K8 *603260 : BarH-LIKE HOMEO BOX GENE 1 *603261 : PHOSPHATIDYLINOSITOL-4-PHOSPHATE 5-KINASE, TYPE II, BETA; PIP5K2B *603262 : 3-PRIME-@PHOSPHOADENOSINE 5-PRIME-PHOSPHOSULFATE SYNTHASE 1; PAPSS1 *603263 : CARBONIC ANHYDRASE XII; CA12 *603264 : RHOMBOID-LIKE; RHBDL *603265 : DEAD RINGER, DROSOPHILA, HOMOLOG-LIKE 1; DRIL1 *603266 : DIABETES MELLITUS, INSULIN-DEPENDENT, 17; IDDM17 *603267 : SMALL OPTIC LOBES, DROSOPHILA, HOMOLOG OF; SOLH *603268 : N-DEACETYLASE/N-SULFOTRANSFERASE 2; NDST2 *603269 : SPLICING FACTOR, ARGININE/SERINE-RICH, 46-KD *603270 : ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL F0 COMPLEX, SUBUNIT B, ISOFORM 1; ATP5F1 *603271 : PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 21; PTPN21 *603272 : CONNECTOR ENHANCER OF KSR, DROSOPHILA, HOMOLOG OF *603273 : TUMOR PROTEIN p63 *603274 : STIMULATOR OF Fe TRANSPORT; SFT *603275 : PHOSPHATIDYLINOSITOL-4-PHOSPHATE 5-KINASE, TYPE I, ALPHA; PIP5K1A *603276 : REGULATOR OF G PROTEIN SIGNALING 5; RGS5 *603277 : CHROMODOMAIN HELICASE DNA-BINDING PROTEIN 4; CHD4 #603278 : FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1; FSGS1 *603279 : EXPANDED REPEAT DOMAIN, CAG/CTG, 1; ERDA1 603280 : PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH HYPOGONADISM *603281 : 2-PRIME,5-PRIME-@OLIGOADENYLATE SYNTHETASE-LIKE; OASL 603282 : ZINC FINGER PROTEIN 204; ZNF204 *603283 : TRIADIN; TRDN *603284 : CEREBRAL CAVERNOUS MALFORMATIONS 2; CCM2 *603285 : CEREBRAL CAVERNOUS MALFORMATIONS 3; CCM3 *603286 : KISS1 METASTASIS SUPPRESSOR; KISS1 603287 : PYRIDOXINE-5-PRIME-PHOSPHATE OXIDASE *603288 : KERATOCAN; KERA *603289 : DEATH-ASSOCIATED PROTEIN KINASE 3; DAPK3 *603290 : SH3 AND MULTIPLE ANKYRIN REPEAT DOMAINS 2; SHANK2 *603291 : BCL2/ADENOVIRUS E1B 19-KD PROTEIN-INTERACTING PROTEIN 1; BNIP1 *603292 : BCL2/ADENOVIRUS E1B 19-KD PROTEIN-INTERACTING PROTEIN 2; BNIP2 *603293 : BCL2/ADENOVIRUS E1B 19-KD PROTEIN-INTERACTING PROTEIN 3; BNIP3 *603294 : MINICHROMOSOME MAINTENANCE 3-ASSOCIATED PROTEIN; MCM3AP *603295 : MOTHERS AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 9; MADH9 *603296 : MEK PARTNER 1 *603297 : DYNEIN, CYTOPLASMIC, HEAVY CHAIN 2; DNCH2 *603298 : PALMITOYL-PROTEIN THIOESTERASE 2; PPT2 *603299 : DYNEIN, HEAVY CHAIN BETA-LIKE *603300 : TUMOR NECROSIS FACTOR-ALPHA-INDUCED PROTEIN 2; TNFAIP2 *603301 : TRANSFORMING GROWTH FACTOR-BETA-INDUCIBLE EARLY GROWTH RESPONSE 2; TIEG2 *603302 : ADENYLATE CYCLASE 9; ADCY9 *603303 : TRF1-INTERACTING, ANKYRIN-RELATED ADP-RIBOSE POLYMERASE; TNKS *603304 : INTERLEUKIN 1 RECEPTOR-ASSOCIATED KINASE 2; IRAK2 *603305 : POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY H, MEMBER 1; KCNH1 *603306 : TRANSCRIPTION FACTOR 21; TCF21 *603307 : BEADED FILAMENT STRUCTURAL PROTEIN 1; BFSP1 *603308 : CATHEPSIN L2; CTSL2 *603309 : CELL DIVISION CYCLE 2-LIKE 5; CDC2L5 *603310 : PHOSPHODIESTERASE 5A; PDE5A *603311 : CELL DIVISION CYCLE 7, S. CEREVISIAE, HOMOLOG-LIKE 1; CDC7L1 *603312 : BUTYROBETAINE-GAMMA,2-OXOGLUTARATE DIOXYGENASE 1; BBOX1 603313 : K+ CHANNEL REGULATOR 1 *603314 : VERY LONG-CHAIN ACYL-CoA SYNTHETASE-RELATED PROTEIN *603315 : FREQUENIN, DROSOPHILA, HOMOLOG OF; FREQ 603316 : CYTIDINE 5-PRIME-MONOPHOSPHATE N-ACETYLNEURAMINIC ACID SYNTHETASE *603317 : PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, EXPRESSED BY GLOMERULAR MESANGIAL CELLS ^603318 : MOVED TO 603345 *603319 : ANNEXIN A9; ANXA9 *603320 : MATRIX METALLOPROTEINASE 23A; MMP23A *603321 : MATRIX METALLOPROTEINASE 23B; MMP23B *603322 : NADH-UBIQUINONE OXIDOREDUCTASE 1 BETA SUBCOMPLEX, 6; NDUFB6 603323 : MUSCULAR DYSTROPHY, CONGENITAL, WITH CEREBELLAR ATROPHY *603324 : GAP JUNCTION PROTEIN, BETA-3; GJB3 *603325 : PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 9B; PPP1R9B *603326 : PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 3D; PPP1R3D *603327 : RAN-BINDING PROTEIN 3; RANBP3 *603328 : MUSASHI, DROSOPHILA, HOMOLOG OF, 1; MSI1 *603329 : PIRIN *603330 : DYNEIN, AXONEMAL, HEAVY CHAIN 9; DNAH9 *603331 : DYNEIN, CYTOPLASMIC, INTERMEDIATE CHAIN 2; DNCI2 *603332 : DYNEIN, AXONEMAL, HEAVY CHAIN 1; DNAH1 *603333 : DYNEIN, AXONEMAL, HEAVY CHAIN 2; DNAH2 *603334 : DYNEIN, AXONEMAL, HEAVY CHAIN 3; DNAH3 *603335 : DYNEIN, AXONEMAL, HEAVY CHAIN 5; DNAH5 *603336 : DYNEIN, AXONEMAL, HEAVY CHAIN 6; DNAH6 *603337 : DYNEIN, AXONEMAL, HEAVY CHAIN 8; DNAH8 ^603338 : MOVED TO 603330 *603339 : DYNEIN, AXONEMAL, HEAVY CHAIN 11; DNAH11 *603340 : DYNEIN, HEAVY CHAIN 12; DNAH12 *603341 : DYNEIN, AXONEMAL, HEAVY CHAIN 14; DNAH14 603342 : SCHIZOPHRENIA 2; SCZD2 *603343 : RNA EXPORT 1, S. POMBE, HOMOLOG OF; RAE1 *603344 : VESICLE DOCKING PROTEIN, 115-KD *603345 : SOLUTE CARRIER FAMILY 4 (SODIUM BICARBONATE COTRANSPORTER), MEMBER 4; SLC4A4 *603346 : NEURONAL PAS DOMAIN PROTEIN 1; NPAS1 *603347 : NEURONAL PAS DOMAIN PROTEIN 2; NPAS2 *603348 : HYPOXIA-INDUCIBLE FACTOR 1, ALPHA SUBUNIT; HIF1A *603349 : ENDOTHELIAL PAS DOMAIN PROTEIN 1; EPAS1 *603350 : 2-PRIME,5-PRIME-@OLIGOADENYLATE SYNTHETASE 2; OAS2 *603351 : 2-PRIME,5-PRIME-@OLIGOADENYLATE SYNTHETASE 3; OAS3 *603352 : BACULOVIRAL IAP REPEAT-CONTAINING PROTEIN 5; BIRC5 *603353 : SOLUTE CARRIER FAMILY 4 (SODIUM BICARBONATE COTRANSPORTER), MEMBER 7; SLC4A7 *603354 : GASTRULATION BRAIN HOMEO BOX 1; GBX1 *603355 : MEMBRANE-BOUND TRANSCRIPTION FACTOR PROTEASE, SITE 1; MBTPS1 *603356 : SIALOMUCIN CD164 *603357 : MEGSIN *603358 : GRACILE SYNDROME *603359 : NADH-UBIQUINONE OXIDOREDUCTASE 1 ALPHA SUBCOMPLEX, 8; NDUFA8 *603360 : PEROXISOME BIOGENESIS FACTOR 16; PEX16 *603361 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 6B; TNFRSF6B *603362 : SH3 DOMAIN, GRB2-LIKE, 3; SH3GL3 *603363 : CGG-BINDING PROTEIN, 20-KD *603364 : SPLICING FACTOR, ARGININE/SERINE-RICH, 3; SFRS3 *603365 : HIRA-INTERACTING PROTEIN 3; HIRIP3 *603366 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 12; TNFRSF12 ^603367 : MOVED TO 300255 *603368 : CYCLIN-DEPENDENT KINASE 6; CDK6 *603369 : CYCLIN-DEPENDENT KINASE INHIBITOR 2C; CDKN2C *603370 : UDP-GLUCOSE DEHYDROGENASE; UGDH *603371 : GLE1, S. CEREVISIAE, HOMOLOG-LIKE; GLE1L *603372 : THYROID-STIMULATING HORMONE RECEPTOR; TSHR #603373 : HYPERTHYROIDISM, FAMILIAL GESTATIONAL ^603374 : MOVED TO 300186 *603375 : SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY A, MEMBER 5; SMARCA5 603376 : LONG-CHAIN FATTY ACIDS, DEFECT IN TRANSPORT OF *603377 : SOLUTE CARRIER FAMILY 22, MEMBER 5; SLC22A5 *603378 : SIN3-ASSOCIATED POLYPEPTIDE, 30-KD; SAP30 *603379 : IQ MOTIF-CONTAINING GTPase-ACTIVATING PROTEIN 1; IQGAP1 *603380 : VERTEBRATE LIN7 HOMOLOG 1 *603381 : FILAMIN B; FLNB 603382 : MutS, E. COLI, HOMOLOG OF, 5; MSH5 *603383 : GLAUCOMA 1, OPEN ANGLE, F; GLC1F *603384 : SYNAPTIC RAS-GTPase-ACTIVATING PROTEIN 1; SYNGAP1 *603385 : AMYLOID BETA PRECURSOR PROTEIN-BINDING PROTEIN 1; APPBP1 *603386 : THYROID CARCINOMA, NONMEDULLARY, WITH CELL OXYPHILIA 603387 : MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT *603388 : GRAVES DISEASE, SUSCEPTIBILITY TO, 2 603389 : OSEBOLD SKELETAL DYSPLASIA/OSTEOLYSIS SYNDROME *603390 : PHOSPHODIESTERASE 8B; PDE8B 603391 : LARYNGOTRACHEAL STENOSIS, PROGRESSIVE, WITH SHORT STATURE AND ARTHROPATHY *603392 : BCL2-INTERACTING KILLER; BIK 603393 : OSTEOSCLEROTIC CHONDRODYSPLASIA, LETHAL, WITH INTRACELLULAR INCLUSIONS 603394 : MICROCEPHALY, SEVERE, WITH SKELETAL ANOMALIES INCLUDING POSTERIOR RIB-GAP DEFECTS *603395 : SPERM-ASSOCIATED ANTIGEN 1; SPAG1 603396 : TONOKI SYNDROME *603397 : ZINC FINGER PROTEIN 282; ZNF282 *603398 : WNT1-INDUCIBLE SIGNALING PATHWAY PROTEIN 1; WISP1 *603399 : WNT1-INDUCIBLE SIGNALING PATHWAY PROTEIN 2; WISP2 *603400 : WNT1-INDUCIBLE SIGNALING PATHWAY PROTEIN 3; WISP3 *603401 : ADAPTIN, BETA-3A; AP3B1 *603402 : ACYL-CoA OXIDASE 3, PRISTANOYL; ACOX3 *603403 : DEAD/H BOX 15; DDX15 *603404 : ZINC FINGER PROTEIN 169; ZNF169 *603405 : DEAD/H BOX 16; DDX16 *603406 : TRANSCRIPTIONAL INTERMEDIARY FACTOR 1; TIF1 *603407 : POLYADENYLATE-BINDING PROTEIN, CYTOPLASMIC, 4; PABPC4 *603408 : FRIZZLED, DROSOPHILA, HOMOLOG OF, 1; FZD1 *603409 : FRIZZLED, DROSOPHILA, HOMOLOG OF, 6; FZD6 *603410 : FRIZZLED, DROSOPHILA, HOMOLOG OF, 7; FZD7 *603411 : EFFECTOR CELL PROTEASE RECEPTOR 1; EPR1 *603412 : PROTEIN KINASE, SERINE/THREONINE, RELATED TO THE MYOTONIC DYSTROPHY PROTEIN KINASE *603413 : TIA1 CYTOTOXIC GRANULE-ASSOCIATED RNA-BINDING PROTEIN-LIKE 1; TIAL1 *603414 : TRANSMEMBRANE 7 SUPERFAMILY, MEMBER 2; TM7SF2 *603415 : SODIUM CHANNEL, VOLTAGE-GATED, TYPE IX, ALPHA SUBUNIT; SCN9A *603416 : ACTIVATOR OF LIVER FUNCTION 1; ALFN1 *603417 : RAB-INTERACTING FACTOR; RABIF *603418 : ALDO-KETO REDUCTASE FAMILY 7, MEMBER A2; AKR7A2 *603419 : SMALL GLUTAMINE-RICH TETRATRICOPEPTIDE REPEAT-CONTAINING PROTEIN; SGT *603420 : CALUMENIN; CALU *603421 : TRANSMEMBRANE PROTEIN WITH EGF-LIKE AND 2 FOLLISTATIN-LIKE DOMAINS 1; TMEFF1 *603422 : LIM DOMAIN PROTEIN RIL *603423 : PR DOMAIN-CONTAINING PROTEIN 1; PRDM1 *603424 : PROTEIN KINASE, INTERFERON-INDUCIBLE DOUBLE-STRANDED RNA-DEPENDENT ACTIVATOR; PRKRA *603425 : ADP-RIBOSYLATION FACTOR-LIKE 1; ARL1 *603426 : PERIOD, DROSOPHILA, HOMOLOG OF, 2; PER2 *603427 : PERIOD, DROSOPHILA, HOMOLOG OF, 3; PER3 *603428 : ZINC FINGER PROTEIN 207; ZNF207 *603429 : ATP-BINDING CASSETTE, SUBFAMILY F, MEMBER 1; ABCF1 *603430 : ZINC FINGER PROTEIN 202; ZNF202 *603431 : WILLIAMS-BEUREN SYNDROME CHROMOSOME REGION 1; WBSCR1 *603432 : CYTOPLASMIC LINKER 2; CYLN2 *603433 : ZINC FINGER PROTEIN 143; ZNF143 *603434 : PHOSPHOPROTEIN ENRICHED IN ASTROCYTES, 15-KD; PEA15 *603435 : GLUTATHIONE PEROXIDASE 5; GPX5 *603436 : ZINC FINGER PROTEIN 205; ZNF205 *603437 : COLD-SHOCK DOMAIN PROTEIN A; CSDA 603438 : RADIOULNAR SYNOSTOSIS WITH SHORT STATURE, MICROCEPHALY, SCOLIOSIS, AND MENTAL RETARDATION 603439 : EXPANSILE BONE LESIONS *603440 : PCTAIRE PROTEIN KINASE 2; PCTK2 *603441 : CYCLIN-DEPENDENT KINASE-LIKE 1; CDKL1 *603442 : CYCLIN-DEPENDENT KINASE-LIKE 2; CDKL2 *603443 : SUPPRESSOR OF ACTIN MUTATIONS 2, S. CEREVISIAE, HOMOLOG-LIKE; SACM2L *603444 : FAR UPSTREAM ELEMENT-BINDING PROTEIN 1; FUBP1 *603445 : KH-TYPE SPLICING REGULATORY PROTEIN; KHSRP 603446 : OROACRAL SYNDROME, VERLOES-KOULISCHER TYPE *603447 : HARAKIRI; HRK *603448 : DISABLED, DROSOPHILA, HOMOLOG OF, 1; DAB1 *603449 : RUVB, E. COLI, HOMOLOG-LIKE 1; RUVBL1 *603450 : LIM DOMAIN-BINDING 2; LDB2 *603451 : LIM DOMAIN-BINDING 1; LDB1 *603452 : MUNC18-1-INTERACTING PROTEIN 2 *603453 : RECEPTOR-INTERACTING SERINE/THREONINE KINASE 1; RIPK1 *603454 : CASP2 AND RIPK1 DOMAIN-CONTAINING ADAPTOR WITH DEATH DOMAIN; CRADD *603455 : RECEPTOR-INTERACTING SERINE/THREONINE KINASE 2; RIPK2 *603456 : DIPHTHAMIDE BIOSYNTHESIS PROTEIN 2, S. CEREVISIAE, HOMOLOG-LIKE 2; DPH2L2 603457 : ARHINIA, CHOANAL ATRESIA, AND MICROPHTHALMIA *603458 : EMBRYONIC LETHAL, ABNORMAL VISION, DROSOPHILA, HOMOLOG-LIKE 3; ELAVL3 ^603459 : MOVED TO 160980 *603460 : CYCLIN-DEPENDENT KINASE 5, REGULATORY SUBUNIT 1; CDK5R1 *603461 : CELL DIVISION CYCLE 16, S. CEREVISIAE, HOMOLOG OF; CDC16 *603462 : CELL DIVISION CYCLE 23; CDC23 603463 : HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARING LOSS *603464 : CYCLIN-DEPENDENT KINASE 10; CDK10 *603465 : CELL DIVISION CYCLE 45, S. CEREVISIAE, HOMOLOG-LIKE; CDC45L *603466 : EMBRYONIC LETHAL, ABNORMAL VISION, DROSOPHILA, HOMOLOG-LIKE 1; ELAVL1 *603467 : FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF ^603468 : MOVED TO 227650 ^603469 : MOVED TO 603240 *603470 : ARGININOSUCCINATE SYNTHETASE; ASS #603471 : CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2 603472 : NEURONAL INTRANUCLEAR INCLUSION DISEASE *603473 : LARGE TUMOR SUPPRESSOR, DROSOPHILA, HOMOLOG OF, 1; LATS1 *603474 : RIBOSOMAL PROTEIN S19; RPS19 *603475 : CHORDIN; CHRD *603476 : cAMP RESPONSE ELEMENT-BINDING PROTEIN-LIKE 2; CREBL2 *603477 : G10 MATERNAL TRANSCRIPT, XENOPUS, HOMOLOG OF *603478 : UBIQUITIN-SPECIFIC PROTEASE 1; USP1 *603479 : EXTRACELLULAR MATRIX PROTEIN 2; ECM2 *603480 : PROTEASOME 26S SUBUNIT, NON-ATPase, 10; PSMD10 *603481 : PROTEASOME 26S SUBUNIT, NON-ATPase, 13; PSMD13 *603482 : BETA-TRANSDUCIN REPEAT-CONTAINING PROTEIN; BTRC *603483 : EUKARYOTIC TRANSLATION INITIATION FACTOR 4E-BINDING PROTEIN 3; EIF4EBP3 *603484 : PROTEIN REGULATING CYTOKINESIS 1; PRC1 *603485 : NITROGEN FIXATION GENE 1; NFS1 *603486 : UBIQUITIN-SPECIFIC PROTEASE 4; USP4 *603487 : MYOSIN, SKELETAL MUSCLE, HEAVY CHAIN 13; MYH13 *603488 : ANGIO-ASSOCIATED MIGRATORY CELL PROTEIN; AAMP *603489 : CARTILAGE INTERMEDIATE LAYER PROTEIN; CILP *603490 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 4; WNT4 *603491 : IMMUNOGLOBULIN SUPERFAMILY, MEMBER 3; IGSF3 *603492 : SIGNALING LYMPHOCYTE ACTIVATION MOLECULE; SLAM *603493 : POTASSIUM CHANNEL, SUBFAMILY K, MEMBER 5; KCNK5 *603494 : NNX3 PROTEIN *603495 : SERINE/THREONINE PROTEIN KINASE 13; STK13 *603496 : DUAL-SPECIFICITY TYROSINE PHOSPHORYLATION-REGULATED KINASE 2; DYRK2 *603497 : DUAL-SPECIFICITY TYROSINE PHOSPHORYLATION-REGULATED KINASE 3; DYRK3 *603498 : SPHINGOMYELIN PHOSPHODIESTERASE 2, NEUTRAL MEMBRANE; SMPD2 *603499 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 11A; TNFRSF11A *603500 : TUMOR NECROSIS FACTOR RECEPTOR 1-ASSOCIATED DEATH DOMAIN PROTEIN; TRADD *603501 : POLY(ADP-RIBOSE) GLYCOHYDROLASE; PARG *603502 : INTERFERON-RELATED DEVELOPMENTAL REGULATOR 1; IFRD1 *603503 : DOLICHYL-PHOSPHATE MANNOSYLTRANSFERASE 1, CATALYTIC SUBUNIT; DPM1 *603504 : CELL DIVISION CYCLE 14, S. CEREVISIAE, HOMOLOG A; CDC14A *603505 : CELL DIVISION CYCLE 14, S. CEREVISIAE, HOMOLOG B; CDC14B *603506 : LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 5; LRP5 *603507 : LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 6; LRP6 *603508 : MYOMESIN 1; MYOM1 *603509 : MYOMESIN 2; MYOM2 *603510 : INSULIN RECEPTOR SUBSTRATE 4; IRS4 *603511 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1D; LGMD1D *603512 : RNA GUANYLYLTRANSFERASE AND 5-PRIME-PHOSPHATASE; RNGTT *603513 : SPASTIC CEREBRAL PALSY, SYMMETRIC, AUTOSOMAL RECESSIVE *603514 : RNA GUANINE-7-METHYLTRANSFERASE; RNMT *603515 : CHORIONIC SOMATOMAMMOTROPIN HORMONE-LIKE 1; CSHL1 *603516 : SPINOCEREBELLAR ATAXIA 10; SCA10 *603517 : B-CELL CLL/LYMPHOMA 10; BCL10 *603518 : TIA1 CYTOTOXIC GRANULE-ASSOCIATED RNA-BINDING PROTEIN; TIA1 *603519 : SURVIVAL OF MOTOR NEURON-RELATED PROTEIN *603520 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE B-DOUBLE PRIME; SNRPB2 *603521 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE A-PRIME; SNRPA1 *603522 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE C; SNRPC 603523 : CHYLOTHORAX, CONGENITAL *603524 : CHROMOSOME CONDENSATION 1-LIKE; CHC1L *603525 : NMYC INTERACTOR; NMI *603526 : METASTASIS-ASSOCIATED GENE 1; MTA1 *603527 : DIPHTHAMIDE BIOSYNTHESIS PROTEIN 2, S. CEREVISIAE, HOMOLOG-LIKE 1; DPH2L1 603528 : DEHYDRATED HEREDITARY STOMATOCYTOSIS, PSEUDOHYPERKALEMIA, AND PERINATAL EDEMA 603529 : DYSERYTHROPOIESIS, CONGENITAL, WITH INTERNUCLEAR CHROMATIN BRIDGES AND ULTRASTRUCTURALLY NORMAL ERYTHROBLAST HETEROCHROMATIN 603530 : LIGHT FIXATION SEIZURE SYNDROME *603531 : ADAPTOR-RELATED PROTEIN COMPLEX 1, SIGMA-1 SUBUNIT; AP1S1 *603532 : ADAPTOR-RELATED PROTEIN COMPLEX 1, SIGMA-2 SUBUNIT; AP1S2 *603533 : ADAPTOR-RELATED PROTEIN COMPLEX 1, GAMMA-1 SUBUNIT; AP1G1 *603534 : ADAPTOR-RELATED PROTEIN COMPLEX 1, GAMMA-2 SUBUNIT; AP1G2 *603535 : ADAPTOR-RELATED PROTEIN COMPLEX 1, MU-1 SUBUNIT; AP1M1 *603536 : FAR UPSTREAM ELEMENT-BINDING PROTEIN 3; FUBP3 *603537 : POTASSIUM CHANNEL, VOLTAGE-GATED, KQT-LIKE SUBFAMILY, MEMBER 4; KCNQ4 *603538 : KYNURENINE 3-MONOOXYGENASE; KMO *603539 : CATHEPSIN F; CTSF *603540 : GAMMA-AMINOBUTYRIC ACID B RECEPTOR 1; GABBR1 *603541 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE F; SNRPF *603542 : SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE G; SNRPG *603543 : LIMB-MAMMARY SYNDROME *603544 : CYCLIN K; CCNK #603545 : ENLARGED VESTIBULAR AQUEDUCT SYNDROME 603546 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH MULTIPLE DISLOCATIONS *603547 : METHYL-CpG-BINDING DOMAIN PROTEIN 2; MBD2 *603548 : CDP-DIACYLGLYCEROL SYNTHASE 1; CDS1 *603549 : CDP-DIACYLGLYCEROL SYNTHASE 2; CDS2 *603550 : EYES ABSENT 4; EYA4 *603551 : HYALURONOGLUCOSAMINIDASE 2; HYAL2 *603552 : HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 #603553 : HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 #603554 : OMENN SYNDROME *603555 : SUPPRESSOR OF TY 4, S. CEREVISIAE, HOMOLOG OF, 1; SUPT4H1 ^603556 : MOVED TO 300171 *603557 : MYOTUBULARIN-RELATED PROTEIN 2; MTMR2 *603558 : MYOTUBULARIN-RELATED PROTEIN 3; MTMR3 *603559 : MYOTUBULARIN-RELATED PROTEIN 4; MTMR4 *603560 : SET-BINDING FACTOR 1; SBF1 *603561 : MYOTUBULARIN-RELATED PROTEIN 6; MTMR6 *603562 : MYOTUBULARIN-RELATED PROTEIN 7; MTMR7 *603563 : SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8 *603564 : DOLICHYL-PHOSPHATE MANNOSYLTRANSFERASE 2, REGULATORY SUBUNIT; DPM2 *603565 : UDP-N-ACETYL-ALPHA-D-GALACTOSAMINE:POLYPEPTIDE N-ACETYLGALACTOSAMINYLTRANSFERASE 4; GALNT4 *603566 : PROTEIN INHIBITOR OF ACTIVATED STAT1; PIAS1 *603567 : PROTEIN INHIBITOR OF ACTIVATED STAT X #603568 : RNA, U73 SMALL NUCLEOLAR; RNU73 603569 : TRACHEOBRONCHIAL STENOSIS, CONGENITAL *603570 : VANIN 1; VNN1 *603571 : VANIN 2; VNN2 603572 : MICROCEPHALY, FACIAL ABNORMALITIES, MICROMELIA, AND MENTAL RETARDATION *603573 : METHYL-CpG-BINDING DOMAIN PROTEIN 3; MBD3 *603574 : METHYL-CpG-BINDING DOMAIN PROTEIN 4; MBD4 *603575 : NONMETASTATIC CELLS 5, PROTEIN EXPRESSED IN; NME5 *603576 : TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY M, MEMBER 1; TRPM1 *603577 : NUCLEOLAR PROTEIN 4; NOL4 *603578 : OVIDUCTAL GLYCOPROTEIN 1; OVGP1 *603579 : SUDD, ASPERGILLUS NIDULANS, HOMOLOG OF; SUDD *603580 : PROTOCADHERIN 8; PCDH8 *603581 : PROTOCADHERIN 9; PCDH9 *603582 : TOPOISOMERASE, DNA, III, BETA; TOP3B *603583 : DISCS LARGE, DROSOPHILA, HOMOLOG OF, 2; DLG2 *603584 : MAP KINASE-ACTIVATING DEATH DOMAIN; MADD 603585 : CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix ^603586 : MOVED TO 603147 603587 : FOLLICULAR ATROPHODERMA, PERIORAL PIGMENTED, WITH MILIA AND EPIDERMOID CYSTS 603588 : PAROTITIS, JUVENILE RECURRENT 603589 : FACIAL DYSMORPHISM, HYPODONTIA, AND CHOROID CALCIFICATION *603590 : ACETYLGLUCOSAMINYLTRANSFERASE-LIKE PROTEIN; LARGE *603591 : UBIQUITIN-SPECIFIC PROTEASE 13; USP13 603592 : XANTHINURIA, TYPE II *603593 : SOLUTE CARRIER FAMILY 7, MEMBER 7; SLC7A7 *603594 : TUMOR NECROSIS FACTOR LIGAND SUPERFAMILY, MEMBER 4; TNFSF4 603595 : CRANIOSYNOSTOSIS WITH ECTOPIA LENTIS #603596 : POLYDACTYLY *603597 : SUPPRESSOR OF CYTOKINE SIGNALING 1 *603598 : TUMOR NECROSIS FACTOR LIGAND SUPERFAMILY, MEMBER 10; TNFSF10 *603599 : CASP8- AND FADD-LIKE APOPTOSIS REGULATOR; CFLAR 603600 : OSTEOMA OF CRANIAL VAULT, FAMILIAL *603601 : PHOSPHATIDYLINOSITOL 3-KINASE, CLASS 2, ALPHA; PIK3C2A *603602 : PHOSPHOLIPASE A2, GROUP IVC; PLA2G4C *603603 : PHOSPHOLIPASE A2, GROUP X; PLA2G10 *603604 : PHOSPHOLIPASE A2, GROUP VI; PLA2G6 *603605 : SMALL INDUCIBLE CYTOKINE SUBFAMILY E, MEMBER 1; SCYE1 *603606 : RIBOSOMAL PROTEIN S6 KINASE, 90-KD, 4; RPS6KA4 *603607 : RIBOSOMAL PROTEIN S6 KINASE, 90-KD, 5; RPS6KA5 *603608 : CARBONYL REDUCTASE 3; CBR3 *603609 : FUCOSE-1-PHOSPHATE GUANYLYLTRANSFERASE; FPGT *603610 : UNC5, C. ELEGANS, HOMOLOG OF, C; UNC5C *603611 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 10A; TNFRSF10A *603612 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 10B; TNFRSF10B *603613 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 10C; TNFRSF10C *603614 : TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 10D; TNFRSF10D *603615 : RAD54, S. CEREVISIAE, HOMOLOG-LIKE; RAD54L *603616 : RABAPTIN 5 *603617 : SOLUTE CARRIER FAMILY 24, MEMBER 1; SLC24A1 *603618 : CELL DIVISION CYCLE 20, S. CEREVISIAE, HOMOLOG OF; CDC20 *603619 : CDH1/HCT1, S. CEREVISIAE, HOMOLOG OF *603620 : PC4- AND SFRS1-INTERACTING PROTEIN 1; PSIP1 *603621 : FORKHEAD ACTIVIN SIGNAL TRANSDUCER 1, XENOPUS, HOMOLOG OF #603622 : DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 17; DFNA17 *603623 : TYROSYL-tRNA SYNTHETASE; YARS *603624 : RIBOSOMAL PROTEIN S2; RPS2 *603625 : LYMPHOCYTE ANTIGEN 6 COMPLEX, LOCUS H; LY6H *603626 : PROTOCADHERIN 1; PCDH1 *603627 : PROTOCADHERIN-GAMMA, SUBFAMILY C, MEMBER 3; PCDHGC3 *603628 : MUSCULIN; MSC #603629 : DEAFNESS, AUTOSOMAL RECESSIVE 21; DFNB21 *603630 : RIBOSOMAL PROTEIN S5; RPS5 *603631 : RIBOSOMAL PROTEIN S9; RPS9 *603632 : RIBOSOMAL PROTEIN S10; RPS10 *603633 : RIBOSOMAL PROTEIN S29; RPS29 *603634 : RIBOSOMAL PROTEIN L5; RPL5 #603635 : RNA, U21 SMALL NUCLEOLAR; RNU21 *603636 : RIBOSOMAL PROTEIN L21; RPL21 *603637 : RIBOSOMAL PROTEIN L27a; RPL27A *603638 : RIBOSOMAL PROTEIN L28; RPL28 *603639 : A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 17; ADAM17 *603640 : A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 19; ADAM19 603641 : NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARING LOSS, AND ENAMEL HYPOPLASIA 603642 : ATRIAL SEPTAL DEFECT, SECUNDUM, WITH VARIOUS CARDIAC AND NONCARDIAC DEFECTS 603643 : SITUS INVERSUS TOTALIS WITH CYSTIC DYSPLASIA OF KIDNEYS AND PANCREAS *603644 : SCO1, S. CEREVISIAE, HOMOLOG OF; SCO1 *603645 : PET112, S. CEREVISIAE, HOMOLOG-LIKE; PET112L *603646 : CYTOCHROME c OXIDASE ASSEMBLY PROTEIN COX15; COX15 *603647 : BCS1, S. CEREVISIAE, HOMOLOG-LIKE; BCS1L *603648 : CYTOCHROME c OXIDASE ASSEMBLY PROTEIN COX11; COX11 *603649 : CONE-ROD DYSTROPHY 7; CORD7 *603650 : BARDET-BIEDL SYNDROME 5; BBS5 *603651 : TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY C, MEMBER 4; TRPC4 *603652 : TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY C, MEMBER 6; TRPC6 ^603653 : REMOVED FROM DATABASE *603654 : SOLUTE CARRIER FAMILY 16, MEMBER 7; SLC16A7 *603655 : GUANINE NUCLEOTIDE-BINDING PROTEIN, GAMMA-TRANSDUCING ACTIVITY POLYPEPTIDE 2; GNGT2 603656 : EXOSTOSIS, DUPUYTREN SUBUNGUAL *603657 : VESICLE-ASSOCIATED MEMBRANE PROTEIN 3; VAMP3 *603658 : RIBOSOMAL PROTEIN S7; RPS7 *603659 : GLUCAGON-LIKE PEPTIDE 2 RECEPTOR; GLP2R *603660 : RIBOSOMAL PROTEIN S12; RPS12 *603661 : RIBOSOMAL PROTEIN L17; RPL17 *603662 : RIBOSOMAL PROTEIN L23; RPL23 *603663 : MENTAL HEALTH WELLNESS 1 603664 : MENTAL HEALTH WELLNESS 2 *603665 : STANNIOCALCIN 2; STC2 *603666 : SYNTAXIN 16; STX16 *603667 : SOLUTE CARRIER FAMILY 25, MEMBER 12; SLC25A12 *603668 : SPLICING FACTOR, ARGININE/SERINE-RICH, 2-INTERACTING PROTEIN; SFRS2IP 603669 : ECCRINE SYRINGOFIBROADENOMATOSIS WITH EYELID ABNORMALITIES 603670 : BLUE NEVI, FAMILIAL MULTIPLE 603671 : ACROMELIC FRONTONASAL DYSOSTOSIS *603672 : CORE-BINDING FACTOR, RUNT DOMAIN, ALPHA SUBUNIT 2, TRANSLOCATED TO, 2; CBFA2T2 *603673 : PATCHED, DROSOPHILA, HOMOLOG OF, 2; PTCH2 *603674 : RIBOSOMAL PROTEIN S15a; RPS15A *603675 : RIBOSOMAL PROTEIN S16; RPS16 ^603676 : MOVED TO 181350 *603677 : MYELIN TRANSCRIPTION FACTOR 2; MYT2 *603678 : DEAFNESS, AUTOSOMAL RECESSIVE 14; DFNB14 *603679 : UBIQUITIN-CONJUGATING ENZYME E2N; UBE2N *603680 : SPINOCEREBELLAR ATAXIA 8; SCA8 *603681 : OTOFERLIN; OTOF *603682 : RIBOSOMAL PROTEIN S20; RPS20 *603683 : RIBOSOMAL PROTEIN S23; RPS23 *603684 : LIPASE, ENDOTHELIAL; LIPG *603685 : RIBOSOMAL PROTEIN S28; RPS28 *603686 : RIBOSOMAL PROTEIN L9; RPL9 *603687 : ALDEHYDE DEHYDROGENASE 1 FAMILY, MEMBER A2; ALDH1A2 *603688 : PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY *603689 : MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT *603690 : ACETYL-CoA TRANSPORTER; ACATN *603691 : GALANIN RECEPTOR 2; GALR2 *603692 : GALANIN RECEPTOR 3; GALR3 *603693 : FRIEND OF GATA2 *603694 : DIABETES MELLITUS, NONINSULIN-DEPENDENT, 3 *603695 : GUANYLATE CYCLASE 1, SOLUBLE, BETA-2; GUCY1B2 *603696 : PEANUT-LIKE 2; PNUTL2 *603697 : ARACHIDONATE 15-LIPOXYGENASE, SECOND TYPE; ALOX15B *603698 : GOLGI-SPECIFIC BREFELDIN-A RESISTANCE FACTOR 1; GBF1 *603699 : WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 11; WNT11 *603700 : ARACHIDON