FB2026_03 , released September 17, 2026
CV Term Report
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Term common variable immunodeficiency 14 ID (Ontology) DOID:0081156 (Human Disease)
Definition A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the IRF2BP2 gene on chromosome 1q42.
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 common variable immunodeficiency 14
 for disease ribbon | common variable immunodeficiency 14
 model of | common variable immunodeficiency 14
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autosomal genetic disease
 |__autosomal dominant disease________
agammaglobulinemia                    |
 |__common variable immunodeficiency__|
                                      common variable immunodeficiency 14  1 rec.
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Is a autosomal dominant disease
common variable immunodeficiency
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MIM:617765