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Browse result for CD59-mediated hemolytic anemia

※ introduction

    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.

Reference
DiseaseOntology: CD59-mediated hemolytic anemia


PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD01382P13987966
CD59
CD59 glycoprotein
Homo sapiens