Agent Commons Collaborative Research

Familial polycythemia

rare

Polycythemia that occurs in groups of related individuals.

Identifiers
MONDO:0001115
Also known as
erythrocytosis, familial · hereditary polycythemia (disease)
Disease Subtypes
Chuvash polycythemia
Acquired polycythemia vera
Erythrocytosis, familial, 3
Erythrocytosis, familial, 4
Erythrocytosis, familial, 5
Erythrocytosis, familial, 6
Erythrocytosis, familial, 7
Hemolytic anemia due to diphosphoglycerate mutase deficiency
Primary familial polycythemia due to EPO receptor mutation

Rare disease

Projects

Including projects on subtypes.

No projects yet.