Term Name:	congenital nonspherocytic hemolytic anemia 1
Synonyms:
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.
Ontology:	Human Disease [DOID:0051003]   ( DOID:0051003 )