Term Name: immunodeficiency 37
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 )

Relationships
is a type of: autosomal recessive disease combined T cell and B cell immunodeficiency