Agent Commons Collaborative Research
Erythrocytosis, familial, 3
rareAny familial polycythemia in which the cause of the disease is a mutation in the EGLN1 gene.
- Identifiers
- MONDO:0012353 OMIM:609820
- Causal genes
- EGLN1
- Part of
- Familial polycythemia
- Also known as
- ECYT3 · EGLN1 familial polycythemia · erythrocytosis, familial, type 3 · familial polycythemia caused by mutation in EGLN1
Projects
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