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Results 1 - 10 of 13 for Familial "erythrocytosis," 1
  1. Familial erythrocytosis 
    ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2 ERYTHROCYTOSIS, FAMILIAL, 3; ...
    https://medlineplus.gov/genetics/condition/familial-erythrocytosis - Genetics
  2. EPAS1 gene 
    ... S, Della Ragione F. The HIF2A gene in familial erythrocytosis. N Engl J Med. 2008 May 1;358(18):1966; author reply 1966-7. No ...
    https://medlineplus.gov/genetics/gene/epas1 - Genetics
  3. EPOR gene 
    ... Rumi E. Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis. Am J Hematol. 2009 Jan;84(1):46-54. doi: 10.1002/ajh.21313. Citation ...
    https://medlineplus.gov/genetics/gene/epor - Genetics
  4. EGLN1 gene 
    ... Rumi E. Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis. Am J Hematol. 2009 Jan;84(1):46-54. doi: 10.1002/ajh.21313. Citation ...
    https://medlineplus.gov/genetics/gene/egln1 - Genetics
  5. VHL gene 
    ... Rumi E. Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis. Am J Hematol. 2009 Jan;84(1):46-54. doi: 10.1002/ajh.21313. Citation ...
    https://medlineplus.gov/genetics/gene/vhl - Genetics
  6. Hypermanganesemia with dystonia 
    ... not show signs and symptoms of the condition. Familial manganese-induced neurotoxicity HMNDYT ... PubMed Mukhopadhyay ...
    https://medlineplus.gov/.../hypermanganesemia-with-dystonia - Genetics
  7. 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
  8. SLC30A10 gene 
    ... been identified in people with hypermanganesemia with dystonia, polycythemia, and cirrhosis (HMDPC, also known as hypermanganesemia with dystonia 1). This inherited disorder is characterized by high levels ...
    https://medlineplus.gov/genetics/gene/slc30a10 - Genetics
  9. Essential thrombocythemia 
    ... When it is inherited, the condition is called familial essential thrombocythemia. Essential thrombocytosis Primary thrombocythemia Primary thrombocytosis Genetic Testing Registry: Thrombocythemia 1 Essential thrombocythemia National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/genetics/condition/essential-thrombocythemia - Genetics
  10. How are genetic conditions and genes named?: MedlinePlus Genetics 
    ... defect that causes the condition (for example, alpha-1 antitrypsin ... polycythemia vera , and cryptogenic cirrhosis ); The parts of the ...
    https://medlineplus.gov/.../mutationsanddisorders/naming - Genetics
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