All diseases

8 entries on 1 page. Showing entries 1 - 8.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05524 EDAID dysplasia, ectodermal, and immunodeficiency (EDAID) - - 1 1 IKBKG, NFKBIA - -
00158 EDAID1 dysplasia, ectodermal, and immunodeficiency, type 1 (EDAID-1, HEDID) 300291 - - - IKBKG - -
00139 ID intellectual disability (ID) - - 2706 2388 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
00163 IMD33 Immunodeficiency 33 300636 XLR 1 1 IKBKG - -
00160 IMDI immunodeficiency, isolated (IMDI) 300584 - 2 2 IKBKG - -
00161 IP incontinentia pigmenti (IP) 308300 XLD 140 61 IKBKG - -
00162 IPD2 invasive pneumococcal disease, recurrent isolated, type 2 (IPD2) 300640 XLD - - IKBKG - -
00159 OLEDAID dysplasia, ectodermal, anhidrotic, lymphedema and immunodeficiency (OLEDAID) 300301 - - - IKBKG - -
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