common variable immunodeficiency 12 Disease Ontology Browser

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Disease Ontology Browser

common variable immunodeficiency 12 (DOID:0081154)
Alliance: disease page
Alt IDs: OMIM:616576
Definition: A common variable immunodeficiency that is characterized by recurrent infections and associated with hypogammaglobulinemia and that has_material_basis_in heterozygous mutation in the NFKB1 gene on chromosome 4q24.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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