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Metadata
ID	DOID:0081141
Name	agammaglobulinemia 9
Definition	An agammaglobulinemia that is characterized by recurrent bacterial infections associated with agammaglobulinemia and absence of circulating B cells and that has_material_basis_in homozygous or compound heterozygous mutation in the SLC39A7 gene on chromosome 6p21. https://pubmed.ncbi.nlm.nih.gov/32384040/
Xrefs	MIM:619693
Parent Relationships	is_a agammaglobulinemia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance