Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616289	OPTIC ATROPHY 9; OPA9	—	—	—
OMIM	OMIM:616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS	—	—	—
OMIM	OMIM:616294	COLE-CARPENTER SYNDROME 2; CLCRP2	—	—	—
OMIM	OMIM:616295	PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS; PLACK	—	—	—
OMIM	OMIM:616298	SINGLETON-MERTEN SYNDROME 2; SGMRT2	—	—	—
OMIM	OMIM:616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D	—	—	—
OMIM	OMIM:616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13	—	—	—
OMIM	OMIM:616304	MYASTHENIC SYNDROME, CONGENITAL, 17; CMS17	—	—	—
OMIM	OMIM:616307	SENIOR-LOKEN SYNDROME 8; SLSN8	—	—	—
OMIM	OMIM:616311	MENTAL RETARDATION, AUTOSOMAL DOMINANT 33; MRD33	—	—	—
OMIM	OMIM:616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A	—	—	—
OMIM	OMIM:616314	MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS2C	—	—	—
OMIM	OMIM:616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A	—	—	—
OMIM	OMIM:616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B	—	—	—
OMIM	OMIM:616323	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C	—	—	—
OMIM	OMIM:616324	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL; CMS4B	—	—	—
OMIM	OMIM:616325	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9	—	—	—
OMIM	OMIM:616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11	—	—	—
OMIM	OMIM:616329	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13; MODY13	—	—	—
OMIM	OMIM:616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18	—	—	—
OMIM	OMIM:616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2	—	—	—
OMIM	OMIM:616335	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3; MCCRP3	—	—	—
OMIM	OMIM:616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29	—	—	—
OMIM	OMIM:616340	DEAFNESS, AUTOSOMAL DOMINANT 67; DFNA67	—	—	—
OMIM	OMIM:616341	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30	—	—	—