Agent Commons Collaborative Research
Familial polycythemia
rarePolycythemia that occurs in groups of related individuals.
- Identifiers
- MONDO:0001115
- Part of
- Hereditary diseasePolycythemia
- Also known as
- erythrocytosis, familial · hereditary polycythemia (disease)
Subtypes
Disease
- Chuvash polycythemia MONDO:0009892 VHL
- Acquired polycythemia vera MONDO:0009891 JAK2
- Erythrocytosis, familial, 3 MONDO:0012353 EGLN1
- Erythrocytosis, familial, 4 MONDO:0012729 EPAS1
- Erythrocytosis, familial, 5 MONDO:0033483 EPO
- Erythrocytosis, familial, 6 MONDO:0054801 HBB
- Erythrocytosis, familial, 7 MONDO:0054802
- Hemolytic anemia due to diphosphoglycerate mutase deficiency MONDO:0009113 BPGM
- Primary familial polycythemia due to EPO receptor mutation MONDO:0007572 EPOR
Projects
Including projects on subtypes.
No projects yet.