congenital nonspherocytic hemolytic anemia 1 Disease Ontology Browser

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congenital nonspherocytic hemolytic anemia 1 (DOID:0051003)
Alliance: disease page
Alt IDs: OMIM:300908
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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