OMIM |
OMIM:617955 |
PHENYTOIN TOXICITY |
— |
— |
— |
OMIM |
OMIM:617956 |
BETA-GLUCOPYRANOSIDE TASTING |
— |
— |
— |
OMIM |
OMIM:617959 |
SPERMATOGENIC FAILURE 24; SPGF24 |
— |
— |
— |
OMIM |
OMIM:617960 |
SPERMATOGENIC FAILURE 25; SPGF25 |
— |
— |
— |
OMIM |
OMIM:617961 |
SPERMATOGENIC FAILURE 26; SPGF26 |
— |
— |
— |
OMIM |
OMIM:617964 |
LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16 |
— |
— |
— |
OMIM |
OMIM:617965 |
SPERMATOGENIC FAILURE 27; SPGF27 |
— |
— |
— |
OMIM |
OMIM:617966 |
LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 7; LDLCQ7 |
— |
— |
— |
OMIM |
OMIM:617967 |
HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES; HYC3 |
— |
— |
— |
OMIM |
OMIM:617970 |
RH-NULL, AMORPH TYPE; RHNA |
— |
— |
— |
OMIM |
OMIM:617971 |
METHEMOGLOBINEMIA, BETA TYPE |
— |
— |
— |
OMIM |
OMIM:617973 |
METHEMOGLOBINEMIA, ALPHA TYPE |
— |
— |
— |
OMIM |
OMIM:617974 |
SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE; SEMDDR |
— |
— |
— |
OMIM |
OMIM:617976 |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63 |
— |
— |
— |
OMIM |
OMIM:617977 |
NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES; NEDSBAS |
— |
— |
— |
OMIM |
OMIM:617980 |
ERYTHROCYTOSIS, FAMILIAL, 6; ECYT6 |
— |
— |
— |
OMIM |
OMIM:617981 |
ERYTHROCYTOSIS, FAMILIAL, 7; ECYT7 |
— |
— |
— |
OMIM |
OMIM:617982 |
VERVERI-BRADY SYNDROME; VERBRAS |
— |
— |
— |
OMIM |
OMIM:617983 |
MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE; MCPH21 |
— |
— |
— |
OMIM |
OMIM:617984 |
MICROCEPHALY 22, PRIMARY, AUTOSOMAL RECESSIVE; MCPH22 |
— |
— |
— |
OMIM |
OMIM:617985 |
MICROCEPHALY 23, PRIMARY, AUTOSOMAL RECESSIVE; MCPH23 |
— |
— |
— |
OMIM |
OMIM:617988 |
JABERI-ELAHI SYNDROME; JABELS |
— |
— |
— |
OMIM |
OMIM:617991 |
DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD |
— |
— |
— |
OMIM |
OMIM:617992 |
DEAFNESS, CONGENITAL HEART DEFECTS, AND POSTERIOR EMBRYOTOXON; DCHE |
— |
— |
— |
OMIM |
OMIM:617993 |
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2; HFTC2 |
— |
— |
— |