About   Help   FAQ
Disease Ontology Browser
familial erythrocytosis 1 (DOID:0060652)
Alliance: disease page
Synonyms: autosomal dominant benign erythrocytosis; ECYT1; primary familial and congenital polycythemia
Alt IDs: OMIM:133100, ICD10CM:D75.0, ORDO:90042
Definition: A primary polycythemia that has_material_basis_in mutation in the gene encoding the erythropoietin receptor. It is characterized by increased serum red blood cell mass and hemoglobin concentration, hypersensitivity of erythroid progenitors to EPO, and low serum levels of EPO.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
03/12/2024
MGI 6.23
The Jackson Laboratory