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Results 1 - 5 of 5 for "Erythrocytosis," "familial," 2
  1. Familial erythrocytosis 
    ... Disorders (NORD) ClinicalTrials.gov ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2 ERYTHROCYTOSIS, FAMILIAL, 3; ECYT3 ERYTHROCYTOSIS, FAMILIAL, 4; ...
    https://medlineplus.gov/genetics/condition/familial-erythrocytosis - Genetics
  2. 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
  3. Polycythemia vera 
    ... present only in certain cells.In rare instances, polycythemia vera has been found to run in families. In some of these families, the risk of developing polycythemia vera appears to have an autosomal dominant pattern ...
    https://medlineplus.gov/genetics/condition/polycythemia-vera - Genetics
  4. Essential thrombocythemia 
    ... Myeloproliferative Disorders. Analysis of the ten-eleven translocation 2 (TET2) gene in familial myeloproliferative neoplasms. Blood. 2009 Aug 20;114(8): ...
    https://medlineplus.gov/genetics/condition/essential-thrombocythemia - Genetics
  5. Primary myelofibrosis 
    ... Myeloproliferative Disorders. Analysis of the ten-eleven translocation 2 (TET2) gene in familial myeloproliferative neoplasms. Blood. 2009 Aug 20;114(8): ...
    https://medlineplus.gov/genetics/condition/primary-myelofibrosis - Genetics