All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00163 AMCBX-1 mycobacteriosis, atypical, familial, X-linked (AMCBX-1) 300636 - - - IKBKG - -
00158 HEDID dysplasia, ectodermal, hypohidrotic, with immune deficiency (HEDID) 300291 - - - IKBKG - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
00160 IMD immunodeficiency, isolated (IMD) 300584 - - - IKBKG - -
00161 IP-2 incontinentia pigmenti, type II (IP-2) 308300 - - - IKBKG - -
00162 IPD-2 invasive pneumococcal disease, recurrent isolated, type 2 (IPD-2) 300640 - - - IKBKG - -
00159 OLEDAID dysplasia, ectodermal, anhidrotic, lymphedema and immunodeficiency (OLEDAID) 300301 - - - IKBKG - -
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