Catalog

Primary inherited erythrocytosis

3A80.0

Link to WHO Definition

Primary inherited erythrocytosis – http://id.who.int/icd/entity/962836252

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.

Parents

Children