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Results 1 - 10 of 21 for "Erythrocytosis," "familial," 4
  1. ... Testing Registry: Erythrocytosis, familial, 3 Genetic Testing Registry: Erythrocytosis, familial, 4 Genetic Testing Registry: Chuvash polycythemia Primary familial polycythemia ...
  2. ... new mutations in the HIF2A gene associated with erythrocytosis. Am J Hematol. 2012 ... of familial and acquired erythrocytosis and thrombocytosis. Am J Hematol. ...
  3. ... c2021. Cold Hands; [cited 2021 Jan 21]; [about 4 screens]. Available from: https://my.clevelandclinic.org/health/symptoms/17861-cold-hands Familydoctor.org [Internet]. Leawood (KS): American Academy of Family Physicians; c2021. Polycythemia Vera; [updated 2018 Oct 29; cited 2021 Jan ...
  4. ... 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 ...
  5. More information and support for people with polycythemia vera and their families can be found at: Leukemia and Lymphoma Society -- www.lls.org/myeloproliferative-neoplasms/polycythemia-vera MPN Research Foundation -- www.mpnresearchfoundation.org/living-with- ...
  6. ... 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 ...
  7. ... MD): U.S. Department of Health and Human Services; Polycythemia Vera; [cited 2022 Jan 4]; [about 14 screens]. Available from: https://www.nhlbi.nih.gov/health-topics/polycythemia-vera National Heart, Lung, and Blood Institute [Internet]. ...
  8. ... 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 ...
  9. ... Testing Registry: Hypermanganesemia with dystonia 2 ... Mukhopadhyay S. Familial manganese-induced neurotoxicity due to mutations in SLC30A10 ...
  10. ... 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: ...
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