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Results 1 - 7 of 7 for "Erythrocytosis," "familial," 4
  1. Familial erythrocytosis 
    ... Testing Registry: Erythrocytosis, familial, 3 Genetic Testing Registry: Erythrocytosis, familial, 4 Genetic Testing Registry: Chuvash polycythemia Primary familial polycythemia ...
    https://medlineplus.gov/genetics/condition/familial-erythrocytosis - Genetics
  2. EPAS1 gene 
    ... new mutations in the HIF2A gene associated with erythrocytosis. Am J Hematol. 2012 ... of familial and acquired erythrocytosis and thrombocytosis. Am J Hematol. ...
    https://medlineplus.gov/genetics/gene/epas1 - Genetics
  3. EGLN1 gene 
    ... the EGLN1 gene have been found to cause familial erythrocytosis, an inherited condition characterized by an increased number ... an elevated risk of abnormal blood clots. When familial erythrocytosis results from EGLN1 gene mutations, it is often ...
    https://medlineplus.gov/genetics/gene/egln1 - Genetics
  4. 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
  5. SLC30A10 gene 
    ... so excess amounts of this element may underlie polycythemia. More About This Health Condition DKFZp547M236 HMDPC solute carrier family 30, member 10 zinc transporter 10 ZnT-10 ...
    https://medlineplus.gov/genetics/gene/slc30a10 - Genetics
  6. Hypermanganesemia with dystonia 
    ... Testing Registry: Hypermanganesemia with dystonia 2 ... Mukhopadhyay S. Familial manganese-induced neurotoxicity due to mutations in SLC30A10 ...
    https://medlineplus.gov/.../hypermanganesemia-with-dystonia - Genetics
  7. Chromosome 20 
    ... S, Dignan P, Soukup S. Partial trisomy 20p: familial occurrence. Am J Med Genet. 2000 Dec 11;95(4):316-9. Citation on PubMed UCSC Genome Browser: ...
    https://medlineplus.gov/genetics/chromosome/20 - Genetics