All diseases

10 entries on 1 page. Showing entries 1 - 10.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02263 CIDX immunodeficiency, combined, X-linked (CIDX) 312863 XLR 1 1 IL2RG - -
04078 CVID11 immunodeficiency, variable, common, type 11 (CVID-11) 615767 AR - - IL21 - -
03109 IBD17 bowel disease, inflammatory, type 17 (IBD-17) 612261 - - - IL23R - -
02403 IDDM10 diabetes mellitus, insulin-dependent, type 10 (IDDM-10) 601942 - - - IL2RA - -
01397 IGER IgEresponsiveness, atopic (IGER) 147050 AD - - HAVCR1, IL21R, IL4R, MS4A2, PHF11, PLA2G7, SELP, SPINK5 - autosomal dominant
02582 IMD41 immunodeficiency, type 41 with lymphoproliferation and autoimmunity 606367 AR - - IL2RA - -
03853 IMD56 Immunodeficiency 56 615207 AR - - IL21R - -
06546 IMD63 Immunodeficiency 63 with lymphoproliferation and autoimmunity 618495 AR - - IL2RB - -
02558 PSORS7 psoriasis, susceptibility to, type 47 605606 - - - IL23R - -
02153 SCIDX1 immunodeficiency, severe combined, X-linked, type 1 (SCIDX-1) 300400 XLR - - IL2RG - -
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