Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616116	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46; MRT46	—	—	—
OMIM	OMIM:616117	CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY; CCDD	—	—	—
OMIM	OMIM:616118	MACULAR DEGENERATION, EARLY-ONSET; EOMD	—	—	—
OMIM	OMIM:616121	GTPase, VERY LARGE INTERFERON-INDUCIBLE, PSEUDOGENE 1; GVINP1	—	—	—
OMIM	OMIM:616126	IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION; IMD38	—	—	—
OMIM	OMIM:616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17	—	—	—
OMIM	OMIM:616138	PERRAULT SYNDROME 5; PRLTS5	—	—	—
OMIM	OMIM:616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27	—	—	—
OMIM	OMIM:616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9	—	—	—
OMIM	OMIM:616145	CATEL-MANZKE SYNDROME; CATMANS	—	—	—
OMIM	OMIM:616151	MACULAR DYSTROPHY, VITELLIFORM, 4; VMD4	—	—	—
OMIM	OMIM:616152	MACULAR DYSTROPHY, VITELLIFORM, 5; VMD5	—	—	—
OMIM	OMIM:616154	PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER; PFCRD	—	—	—
OMIM	OMIM:616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S	—	—	—
OMIM	OMIM:616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31	—	—	—
OMIM	OMIM:616165	NEMALINE MYOPATHY 10; NEM10	—	—	—
OMIM	OMIM:616166	AORTIC ANEURYSM, FAMILIAL THORACIC 9; AAT9	—	—	—
OMIM	OMIM:616170	MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT; CCMD	—	—	—
OMIM	OMIM:616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2	—	—	—
OMIM	OMIM:616172	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9; GEFSP9	—	—	—
OMIM	OMIM:616176	BLEEDING DISORDER, PLATELET-TYPE, 19; BDPLT19	—	—	—
OMIM	OMIM:616182	CHRONIC MOUNTAIN SICKNESS, SUSCEPTIBILITY TO	—	—	—
OMIM	OMIM:616185	OVARIAN DYSGENESIS 4; ODG4	—	—	—
OMIM	OMIM:616187	EPILEPSY, PROGRESSIVE MYOCLONIC 7; EPM7	—	—	—
OMIM	OMIM:616188	RETINAL DYSTROPHY AND OBESITY; RDOB	—	—	—