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Metadata
ID	DOID:0081152
Name	common variable immunodeficiency 10
Definition	A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the NFKB2 gene on chromosome 10q24. https://pubmed.ncbi.nlm.nih.gov/24140114/
Xrefs	MIM:615577
Parent Relationships	is_a common variable immunodeficiency is_a autosomal dominant disease
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance