OMIM
Db Link Name Definition Comment Is a
OMIM OMIM:617023 RETINITIS PIGMENTOSA 75; RP75
OMIM OMIM:617024 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H; CSNB1H
OMIM OMIM:617025 NEVUS COMEDONICUS; NC
OMIM OMIM:617026 PONTOCEREBELLAR HYPOPLASIA, TYPE 2F; PCH2F
OMIM OMIM:617027 HYPERALDOSTERONISM, FAMILIAL, TYPE IV; HALD4
OMIM OMIM:617028 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54; MRT54
OMIM OMIM:617030 MYOPATHY, DISTAL, 5; MPD5
OMIM OMIM:617035 PATENT DUCTUS ARTERIOSUS 2; PDA2
OMIM OMIM:617039 PATENT DUCTUS ARTERIOSUS 3; PDA3
OMIM OMIM:617041 DUANE RETRACTION SYNDROME 3 WITH OR WITHOUT DEAFNESS; DURS3
OMIM OMIM:617044 SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS; SDDHD
OMIM OMIM:617046 SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE; SPG77
OMIM OMIM:617047 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26; CMH26
OMIM OMIM:617049 CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5; PFIC5
OMIM OMIM:617050 HERMANSKY-PUDLAK SYNDROME 10; HPS10
OMIM OMIM:617051 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55; MRT55
OMIM OMIM:617052 BONE MARROW FAILURE SYNDROME 3; BMFS3
OMIM OMIM:617053 MIRAGE SYNDROME; MIRAGE
OMIM OMIM:617054 STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET; SNDC
OMIM OMIM:617055 CRISPONI/COLD-INDUCED SWEATING SYNDROME 3; CISS3
OMIM OMIM:617056 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4
OMIM OMIM:617061 MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44
OMIM OMIM:617062 OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS
OMIM OMIM:617063 MEIER-GORLIN SYNDROME 7; MGORS7
OMIM OMIM:617065 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40; EIEE40