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Results 1 - 5 of 5 for Familial erythrocytosis
  1. Familial erythrocytosis 
    Familial erythrocytosis is an inherited condition characterized by an increased number of red blood cells (erythrocytes). The primary function of these cells is ...
    https://medlineplus.gov/genetics/condition/familial-erythrocytosis - Genetics
  2. Polycythemia vera 
    ... to run in families. In some of these families, the risk of developing polycythemia vera appears to have an autosomal dominant pattern ... condition in familial cases is unknown. In these families, people seem to inherit an increased risk of ... itself. Osler-Vaquez disease ...
    https://medlineplus.gov/genetics/condition/polycythemia-vera - Genetics
  3. Hypermanganesemia with dystonia 
    ... not show signs and symptoms of the condition. Familial manganese-induced neurotoxicity HMNDYT Genetic Testing Registry: Hypermanganesemia with dystonia 2 Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/.../hypermanganesemia-with-dystonia - Genetics
  4. Essential thrombocythemia 
    ... RL. TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis. Leukemia. 2009 May; ...
    https://medlineplus.gov/genetics/condition/essential-thrombocythemia - Genetics
  5. Primary myelofibrosis 
    ... RL. TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis. Leukemia. 2009 May; ...
    https://medlineplus.gov/genetics/condition/primary-myelofibrosis - Genetics