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| Term | common variable immunodeficiency 2 | ID (Ontology) | DOID:0081145 (Human Disease) |
| Definition | A common variable immunodeficiency that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the TNFRSF13B gene, which encodes the transmembrane activator and CAML interactor (TACI), on chromosome 17p11.2. | ||
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autosomal recessive disease |__common variable immunodeficiency__ autosomal genetic disease | |__autosomal dominant disease________| agammaglobulinemia | |__common variable immunodeficiency__| common variable immunodeficiency 2 |
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| Is a |
autosomal dominant disease common variable immunodeficiency |
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| MIM:240500 | |||