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Summary Literature (0)
DOID:0111846 - X-linked congenital hemolytic anemia


Disease Ontology Definition:A congenital hemolytic anemia characterized by mild congenital hemolytic anemia without morphologic red cell abnormalities that has_material_basis_in hemizygous mutation in the ATP11C gene on chromosome Xq27.1.

Synonyms:

Xenbase Genes : atp11c



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): congenital hemolytic anemia (is_a)