Erythrocytosis, familial, 3

Any familial polycythemia in which the cause of the disease is a mutation in the EGLN1 gene.

Also known as: EGLN1 familial polycythemia, erythrocytosis, familial, 3, erythrocytosis, familial, type 3, familial polycythemia caused by mutation in EGLN1, ECYT3

1 clinical trial for this condition and its sub-types.