congenital nonspherocytic hemolytic anemia 5 Disease Ontology Browser

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congenital nonspherocytic hemolytic anemia 5 (DOID:0051006)
Alliance: disease page
Alt IDs: OMIM:235700
Definition: A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the HK1 gene, which encodes a form of hexokinase, on chromosome 10q22.

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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