OMIM
Db Link Name Definition Comment Is a
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