Synonyms: Chuvash polycythemia | Von Hippel-Lindau-dependent polycythemia
Chuvash erythrocytosis is a rare genetic congenital secondary polycythemia disorder characterized by increased hemoglobin hematocrit and erythropoietin serum levels and normal oxygen affinity which usually manifests with headache dizziness dyspnea and/or plethora. Patients present an increased risk of hemorrhage thrombosis and early death.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2026
Newly diagnosed with
Chuvash erythrocytosis?
Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.
Clinical Trials
For a list of clinical trials in this disease area, please click here.
