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	—	—	—