Disease

familial erythrocytosis 8

Definition
A primary polycythemia characterized by erythrocytosis and in some cases hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the BPGM gene on chromosome 7q33.
Synonyms
  • bisphosphoglycerate mutase deficiency
  • bisphosphoglyceromutase deficiency
Cross References
Parent Terms
Child Terms
None
Sources of Associations

Associated Genes

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Associated Models