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Metadata
ID	DOID:0111939
Name	immunodeficiency 37
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. https://pubmed.ncbi.nlm.nih.gov/25365219/
Xrefs	MIM:616098 UMLS_CUI:C4015195
Synonyms	IMD37 [EXACT]
Parent Relationships	is_a combined T cell and B cell immunodeficiency is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance