3A80.0 Primary inherited erythrocytosis
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
A disease caused by genetically inherited factors leading to changes in the concentration of red blood cells. This disease is characterised by having a high concentration of red blood cells in the body leading to slow flow of blood. Confirmation is by identification of mutations by genetic testing.
synonyms
- Primary inherited erythrocytosis
- Primary familial polycythaemia
- Primary inherited polycythaemia
- Polycythaemia due to HIF2A mutation
- Polycythaemia due to PHD2 mutation
- Polycythaemia due to VHL mutation
- Chuvash polycythaemia
- Von Hippel-Lindau-dependent polycythaemia
- Chuvash erythrocytosis
- Primary familial polycythaemia due to EPOR mutation
- Primary familial polycythaemia due to other mutations
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com