FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term common variable immunodeficiency 13 ID (Ontology) DOID:0081155 (Human Disease)
Definition A common variable immunodeficiency that is characterized by recurrent bacterial infections, mainly affecting the respiratory tract, and associated with hypogammaglobulinemia and decreased numbers of B cells and that has_material_basis_in heterozygous mutation in the IKZF1 gene on chromosome 7p12.
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 Genes
 common variable immunodeficiency 13       1
 for disease ribbon | common variable immunodeficiency 13       1
 model of | common variable immunodeficiency 13       1
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autosomal recessive disease
 |__common variable immunodeficiency__
autosomal genetic disease             |
 |__autosomal dominant disease________|
agammaglobulinemia                    |
 |__common variable immunodeficiency__|
                                      common variable immunodeficiency 13  1 rec.
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Is a autosomal dominant disease
common variable immunodeficiency
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MIM:616873