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 |
— |
— |
— |