All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01861 CVID2 immunodeficiency, variable, common, type 2 (CVID-2) 240500 AD;AR - - CD19, CR2, ICOS, TNFRSF13B, TNFRSF13C - -
02856 IGAD2 immunoglobulin A deficiency, type 2 (IGAD-2) 609529 - - - TNFRSF13B - -
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