All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01145 EIEE14 encephalopathy, epileptic, early infantile, type 14 (EIEE-14) 614959 AD 0 0 KCNT1 - -
01146 ENFL5 epilepsy, frontal lobe, nocturnal, type 5 (ENFL-5) 615005 AD 0 0 KCNT1 - -
00139 ID intellectual disability (ID) - - 2210 1907 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 542 more - -
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