All diseases

9 entries on 1 page. Showing entries 1 - 9.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02582 - Interleukin 2 receptor, alpha, deficiency of 606367 - 0 0 IL2RA - -
03853 - IL21R immunodeficiency 615207 - 0 0 IL21R - -
02263 CIDX immunodeficiency, combined, X-linked (CIDX) 312863 - 0 0 IL2RG - -
04078 CVID-11 immunodeficiency, variable, common, type 11 (CVID-11) 615767 - 0 0 IL21 - -
03109 IBD-17 bowel disease, inflammatory, type 17 (IBD-17) 612261 - 0 0 IL23R - -
02403 IDDM-10 diabetes mellitus, insulin-dependent, type 10 (IDDM-10) 601942 - 0 0 IL2RA - -
01397 IGER IgEresponsiveness, atopic (IGER) 147050 - 0 0 HAVCR1, IL21R, IL4R, MS4A2, PHF11, PLA2G7, SELP, SPINK5 - autosomal dominant
02558 PSORS-7 psoriasis, susceptibility to, type 47 605606 - 0 0 IL23R - -
02153 SCIDX-1 immunodeficiency, severe combined, X-linked, type 1 (SCIDX-1) 300400 - 0 0 IL2RG - -
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