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
03489 - OKT4 epitope deficiency 613949 - - - CD4 - -
03204 AHUS2 hemolyticuremic syndrome, atypical, type 2 (AHUS2) 612922 AD;AR - - CD46 - -
02243 HIGM1 immunodeficiency, with hyper IgM, type 1 (HIGM-1) 308230 XLR 3 3 CD40LG - -
02611 HIGM3 immunodeficiency, with hyper IgM, type 3 (HIGM-3) 606843 AR 1 - CD40 - -
00139 ID intellectual disability (ID) - - 2794 2475 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 556 more - -
02813 IN blood group system, Indian 609027 - - - CD44 - -
03753 MAHCJ aciduria, methylmalonic, and homocystinuria, cblJ type 614857 AR 1 1 ABCD4 - -
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