Term Name: | immunodeficiency 37 |
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Synonyms: | IMD37 |
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. |
Ontology: | Human Disease [DOID:0111939] ( DOID:0111939 ) |