OMIM
Db Link Name Definition Comment Is a
OMIM OMIM:615877 MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS
OMIM OMIM:615878 CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4; PFIC4
OMIM OMIM:615879 TATTON-BROWN-RAHMAN SYNDROME; TBRS
OMIM OMIM:615881 PLASMA TRIGLYCERIDE LEVEL QUANTITATIVE TRAIT LOCUS; TGQTL
OMIM OMIM:615883 MYOPATHY, TUBULAR AGGREGATE, 2; TAM2
OMIM OMIM:615885 HYPOTRICHOSIS 12; HYPT12
OMIM OMIM:615887 AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5; AI2A5
OMIM OMIM:615888 BLEEDING DISORDER, PLATELET-TYPE, 18; BDPLT18
OMIM OMIM:615889 LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP
OMIM OMIM:615892 OROFACIAL CLEFT 14; OFC14
OMIM OMIM:615895 POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1
OMIM OMIM:615896 HYPOTRICHOSIS 13; HYPT13
OMIM OMIM:615897 IMMUNODEFICIENCY 24; IMD24
OMIM OMIM:615905 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25; EIEE25
OMIM OMIM:615907 LYMPHEDEMA, HEREDITARY, ID; LMPH1D
OMIM OMIM:615909 DIAMOND-BLACKFAN ANEMIA 13; DBA13
OMIM OMIM:615911 FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2
OMIM OMIM:615916 CARDIOMYOPATHY, DILATED, 1NN; CMD1NN
OMIM OMIM:615917 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20; COXPD20
OMIM OMIM:615918 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21; COXPD21
OMIM OMIM:615919 ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2
OMIM OMIM:615922 RETINITIS PIGMENTOSA 70; RP70
OMIM OMIM:615923 EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE; ECDM
OMIM OMIM:615924 ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD
OMIM OMIM:615925 GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL; GHDP