OMIM
Db Link Name Definition Comment Is a
OMIM OMIM:617862 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA
OMIM OMIM:617864 NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA
OMIM OMIM:617865 NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA
OMIM OMIM:617866 SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18
OMIM OMIM:617871 RETINITIS PIGMENTOSA 81; RP81
OMIM OMIM:617872 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34
OMIM OMIM:617873 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35
OMIM OMIM:617874 POLYCYSTIC LIVER DISEASE 3 WITH OR WITHOUT KIDNEY CYSTS; PCLD3
OMIM OMIM:617875 POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS; PCLD4
OMIM OMIM:617877 SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC
OMIM OMIM:617879 LEBER CONGENITAL AMAUROSIS WITH EARLY-ONSET DEAFNESS; LCAEOD
OMIM OMIM:617882 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG
OMIM OMIM:617883 FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS
OMIM OMIM:617885 BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19; BMIQ19
OMIM OMIM:617892 AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24; ALS24
OMIM OMIM:617895 SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19
OMIM OMIM:617898 MULTIPLE SYNOSTOSES SYNDROME 4; SYNS4
OMIM OMIM:617899 LEUKODYSTROPHY, HYPOMYELINATING, 14; HLD14
OMIM OMIM:617900 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8
OMIM OMIM:617903 NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS
OMIM OMIM:617904 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59; EIEE59
OMIM OMIM:617907 ERYTHROCYTOSIS, FAMILIAL, 5; ECYT5
OMIM OMIM:617911 DIAMOND-BLACKFAN ANEMIA-LIKE; DBAL
OMIM OMIM:617912 CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5
OMIM OMIM:617913 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR