familial erythrocytosis 2 (DOID:0060474)
Alliance: disease page
Synonyms: autosomal recessive benign erythrocytosis; Chuvash erythromatosis; Chuvash polycythemia; Chuvash type polycythemia; ECYT2
Alt IDs: OMIM:263400, ICD10CM:D75.1, ORDO:238557
Definition: A primary polycythemia that has_material_basis_in homozygous or compound heterozygous mutation in the VHL gene (608537) on chromosome 3p25.