OMIM
Db Link Name Definition Comment Is a
OMIM OMIM:618049 PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2
OMIM OMIM:618050 MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57
OMIM OMIM:618052 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 27; CMH27
OMIM OMIM:618056 NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS
OMIM OMIM:618057 DRUG METABOLISM, ALTERED, CES1-RELATED
OMIM OMIM:618060 INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA
OMIM OMIM:618061 POLYCYSTIC KIDNEY DISEASE 6 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD6
OMIM OMIM:618063 CILIARY DYSKINESIA, PRIMARY, 38; CILD38
OMIM OMIM:618065 PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D
OMIM OMIM:618067 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66
OMIM OMIM:618074 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 6; FAME6
OMIM OMIM:618075 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 7; FAME7
OMIM OMIM:618076 NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG
OMIM OMIM:618077 INFLAMMATORY BOWEL DISEASE 29; IBD29
OMIM OMIM:618078 OVARIAN DYSGENESIS 6; ODG6
OMIM OMIM:618079 LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 8; LDLCQ8
OMIM OMIM:618084 PEELING SKIN SYNDROME 6; PSS6
OMIM OMIM:618086 SPERMATOGENIC FAILURE 28; SPGF28
OMIM OMIM:618087 SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND
OMIM OMIM:618088 NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS
OMIM OMIM:618089 INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA
OMIM OMIM:618090 NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC