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Up to: Inborn errors of metabolism · Familial hemolytic anemia · Anemia due to erythrocyte enzyme disorder
Hemolytic anemia due to diphosphoglycerate mutase deficiency
A rare, autosomal recessive, inherited disorder caused by mutation of the BPGM gene. It is characterized by hemolytic anemia and splenomegaly.
This condition has no sub-types.