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Disease Ontology Browser
immunodeficiency 37 (DOID:0111939)
Alliance: disease page
Synonyms: IMD37
Alt IDs: OMIM:616098, UMLS_CUI:C4015195
Definition: A combined T cell and B cell immunodeficiency characterized by hypogammaglobulinemia with profoundly reduced memory B cells and memory T cells and increased numbers of circulating naive lymphocytes that has_material_basis_in homozygous or compound heterozygous mutation in the BCL10 gene on chromosome 1p22.3.


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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last database update
09/19/2023
MGI 6.22
The Jackson Laboratory