Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:617113	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43; EIEE43	—	—	—
OMIM	OMIM:617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7	—	—	—
OMIM	OMIM:617115	PEELING SKIN SYNDROME 5; PSS5	—	—	—
OMIM	OMIM:617116	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2; FFEVF2	—	—	—
OMIM	OMIM:617118	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3; FFEVF3	—	—	—
OMIM	OMIM:617119	BARDET-BIEDL SYNDROME 20; BBS20	—	—	—
OMIM	OMIM:617120	JOUBERT SYNDROME 27; JBTS27	—	—	—
OMIM	OMIM:617121	JOUBERT SYNDROME 28; JBTS28	—	—	—
OMIM	OMIM:617123	RETINITIS PIGMENTOSA 76; RP76	—	—	—
OMIM	OMIM:617125	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 56; MRT56	—	—	—
OMIM	OMIM:617126	ALAZAMI-YUAN SYNDROME; ALYUS	—	—	—
OMIM	OMIM:617127	OROFACIODIGITAL SYNDROME XV; OFD15	—	—	—
OMIM	OMIM:617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44; EIEE44	—	—	—
OMIM	OMIM:617133	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24; SCAR24	—	—	—
OMIM	OMIM:617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2	—	—	—
OMIM	OMIM:617140	ZTTK SYNDROME; ZTTKS	—	—	—
OMIM	OMIM:617141	ANIRIDIA 2; AN2	—	—	—
OMIM	OMIM:617142	ANIRIDIA 3; AN3	—	—	—
OMIM	OMIM:617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20	—	—	—
OMIM	OMIM:617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET; NADGP	—	—	—
OMIM	OMIM:617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH; DAIPT	—	—	—
OMIM	OMIM:617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45; EIEE45	—	—	—
OMIM	OMIM:617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15	—	—	—
OMIM	OMIM:617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS	—	—	—
OMIM	OMIM:617158	MYOPATHY, DISTAL, WITH RIMMED VACUOLES; DMRV	—	—	—