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

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