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.

Also known as: diphosphoglycerate phosphatase deficiency, erythrocytosis, familial, 8, BPGM deficiency, DPGM deficiency, bisphosphoglycerate mutase deficiency, bisphosphoglyceromutase deficiency, diphosphoglycerate mutase deficiency of erythrocyte

64 clinical trials for this condition and its sub-types.