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Metadata
ID	DOID:0081136
Name	agammaglobulinemia 1
Definition	An agammaglobulinemia that has_material_basis_in homozygous or compound heterozygous mutation in the mu heavy-chain gene (IGHM) on chromosome 14q32. https://pubmed.ncbi.nlm.nih.gov/32384040/
Xrefs	MIM:601495
Parent Relationships	is_a agammaglobulinemia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance