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Results 1 - 10 of 15 for Erythrocytosis
  1. Familial erythrocytosis 
    Familial erythrocytosis is an inherited condition characterized by an increased number of red blood cells (erythrocytes). The primary function of these cells is ...
    https://medlineplus.gov/genetics/condition/familial-erythrocytosis - Genetics
  2. Polycythemia vera 
    Polycythemia vera is a condition characterized by an increased number of red blood cells in the bloodstream. Affected individuals may also have excess white blood ...
    https://medlineplus.gov/genetics/condition/polycythemia-vera - Genetics
  3. Hypermanganesemia with dystonia 
    ... of hypermanganesemia with dystonia, called hypermanganesemia with dystonia, polycythemia, and cirrhosis (HMDPC) and hypermanganesemia with dystonia 2, ...
    https://medlineplus.gov/.../hypermanganesemia-with-dystonia - Genetics
  4. EPOR gene 
    ... EPOR gene have been found to cause familial erythrocytosis, an inherited condition characterized by an increased number ... elevated risk of abnormal blood clots. When familial erythrocytosis results from EPOR gene mutations, it is often ...
    https://medlineplus.gov/genetics/gene/epor - Genetics
  5. EPAS1 gene 
    ... EPAS1 gene have been found to cause familial erythrocytosis, an inherited condition characterized by an increased number ... elevated risk of abnormal blood clots. When familial erythrocytosis results from EPAS1 gene mutations, it is often ...
    https://medlineplus.gov/genetics/gene/epas1 - Genetics
  6. EGLN1 gene 
    ... EGLN1 gene have been found to cause familial erythrocytosis, an inherited condition characterized by an increased number ... elevated risk of abnormal blood clots. When familial erythrocytosis results from EGLN1 gene mutations, it is often ...
    https://medlineplus.gov/genetics/gene/egln1 - Genetics
  7. VHL gene 
    ... VHL gene have been found to cause familial erythrocytosis, a condition characterized by an increased number of ... elevated risk of abnormal blood clots. When familial erythrocytosis results from VHL gene mutations, it is often ...
    https://medlineplus.gov/genetics/gene/vhl - Genetics
  8. SLC30A10 gene 
    ... been identified in people with hypermanganesemia with dystonia, polycythemia, and cirrhosis (HMDPC, also known as hypermanganesemia with ... dystonia); an increased number of red blood cells (polycythemia); and liver abnormalities, including irreversible liver disease (cirrhosis). ...
    https://medlineplus.gov/genetics/gene/slc30a10 - Genetics
  9. JAK2 gene 
    ... mutations in the JAK2 gene are associated with polycythemia vera, a disorder characterized by uncontrolled blood cell ... found in approximately 96 percent of people with polycythemia vera. About 3 percent of affected individuals have ...
    https://medlineplus.gov/genetics/gene/jak2 - Genetics
  10. TET2 gene 
    ... mutations in the TET2 gene are associated with polycythemia vera, a disorder characterized by uncontrolled blood cell ... found in approximately 16 percent of people with polycythemia vera. It is unclear what role these mutations ...
    https://medlineplus.gov/genetics/gene/tet2 - Genetics
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