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
00230 AS Angelman syndrome (AS) 105830 AD 133 139 CDKL5, MECP2, UBE3A - -
00067 EIEE2 encephalopathy, epileptic, early infantile, type 2 (EIEE2) 300672 XLD 62 56 CDKL5 - -
00139 ID intellectual disability (ID) - - 2351 2050 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 543 more - -
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