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	—	—	—