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Results 1 - 6 of 6 for "Erythrocytosis," "familial," 2
  1. EGLN1 gene 
    ... TR, Maxwell PH, McMullin MF, Lee FS. A family with erythrocytosis establishes a role for prolyl hydroxylase domain protein 2 in oxygen homeostasis. Proc Natl Acad Sci U ...
    https://medlineplus.gov/genetics/gene/egln1 - Genetics
  2. EPOR gene 
    ... la Chapelle A. Erythropoietin receptor mutations associated with familial erythrocytosis cause hypersensitivity to erythropoietin in the heterozygous state. Blood. 1999 Oct 1;94(7):2530-2. Citation on PubMed Watowich SS. The erythropoietin receptor: ...
    https://medlineplus.gov/genetics/gene/epor - Genetics
  3. EPAS1 gene 
    ... 1002/ajh.21313. Citation on PubMed Percy MJ. Familial erythrocytosis arising from a gain-of-function mutation in the HIF2A gene of the oxygen sensing pathway. Ulster Med J. 2008 May;77(2):86-8. Citation on PubMed or Free article ...
    https://medlineplus.gov/genetics/gene/epas1 - Genetics
  4. VHL gene 
    ... Rumi E. Genetic origins and clinical phenotype of familial and acquired ... Hematology. 2007 Apr;12(2):131-9. doi: 10.1080/10245330601111979. Citation on ...
    https://medlineplus.gov/genetics/gene/vhl - Genetics
  5. TET2 gene 
    ... probable methylcytosine dioxygenase TET2 isoform b tet oncogene family member 2 TET2_HUMAN Tests of TET2 PubMed TET METHYLCYTOSINE ... 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/gene/tet2 - Genetics
  6. 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