X-linked congenital hemolytic anemia Disease Ontology Browser

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Disease Ontology Browser

X-linked congenital hemolytic anemia (DOID:0111846)
Alliance: disease page
Alt IDs: OMIM:301015
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.

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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