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Disease Ontology Browser
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.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory