Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7	—	—	—
OMIM	OMIM:616345	IMMUNODEFICIENCY 39; IMD39	—	—	—
OMIM	OMIM:616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31	—	—	—
OMIM	OMIM:616351	MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34	—	—	—
OMIM	OMIM:616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6; DKCB6	—	—	—
OMIM	OMIM:616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20	—	—	—
OMIM	OMIM:616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35	—	—	—
OMIM	OMIM:616357	DEAFNESS, AUTOSOMAL DOMINANT 40; DFNA40	—	—	—
OMIM	OMIM:616361	PARKINSON DISEASE 21; PARK21	—	—	—
OMIM	OMIM:616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36	—	—	—
OMIM	OMIM:616364	WHITE-SUTTON SYNDROME; WHSUS	—	—	—
OMIM	OMIM:616366	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32; EIEE32	—	—	—
OMIM	OMIM:616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA	—	—	—
OMIM	OMIM:616368	CHOPS SYNDROME; CHOPS	—	—	—
OMIM	OMIM:616369	MOVED TO 243605	—	—	—
OMIM	OMIM:616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4	—	—	—
OMIM	OMIM:616371	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 4; PFBMFT4	—	—	—
OMIM	OMIM:616373	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 3; PFBMFT3	—	—	—
OMIM	OMIM:616389	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G; CSNB1G	—	—	—
OMIM	OMIM:616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE; TTD2	—	—	—
OMIM	OMIM:616392	SKINT1-LIKE PSEUDOGENE; SKINTL	—	—	—
OMIM	OMIM:616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38	—	—	—
OMIM	OMIM:616394	RETINITIS PIGMENTOSA 71; RP71	—	—	—
OMIM	OMIM:616395	TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3	—	—	—
OMIM	OMIM:616398	DYSTONIA 26, MYOCLONIC; DYT26	—	—	—