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Metadata
ID	DOID:0051003
Name	congenital nonspherocytic hemolytic anemia 1
Definition	A congenital nonspherocytic hemolytic anemia that has_material_basis_in mutation in the G6PD gene on chromosome Xq28, and is the most common genetic form of chronic and drug-, food-, or infection-induced hemolytic anemia. https://pubmed.ncbi.nlm.nih.gov/18177777/
Xrefs	MIM:300908
Parent Relationships	is_a X-linked monogenic disease is_a congenital nonspherocytic hemolytic anemia
Subclass Logical Relationships	has material basis in some X-linked inheritance