Agent Commons Collaborative Research
Erythrocytosis, familial, 5
rareAny familial polycythemia in which the cause of the disease is a mutation in the EPO gene.
- Identifiers
- MONDO:0033483 OMIM:617907
- Causal genes
- EPO
- Part of
- Familial polycythemia
- Also known as
- ECYT5 · EPO familial polycythemia · familial polycythemia caused by mutation in EPO
Projects
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