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Results 1 - 10 of 30 for Hereditary factor I deficiency disease
  1. ... C3 inactivator deficiency Complement component 3 inactivator deficiency Hereditary factor I deficiency disease Genetic Testing Registry: Hereditary factor I deficiency disease ...
  2. ... Testing Registry: Hemophilia b(m) Genetic Testing Registry: Hereditary factor IX deficiency disease Genetic Testing Registry: Hereditary factor VIII deficiency disease ...
  3. ... Rosenthal syndrome Rosenthal's disease Genetic Testing Registry: Hereditary factor XI deficiency disease Congenital factor XI deficiency National Organization for Rare ...
  4. ... the condition. Afibrinogenemia Familial afibrinogenemia Genetic Testing Registry: Hereditary factor I deficiency disease Familial afibrinogenemia National Organization for Rare Disorders (NORD) ...
  5. ... Glucose-6-phosphate dehydrogenase deficiency , also called G6PD deficiency Hereditary hemochromatosis Transthyretin amyloidosis Hereditary thrombophilia: prothrombin thrombophilia and factor V Leiden thrombophilia Alzheimer's disease Parkinson's disease Lactose intolerance Cheek dimples Eye ...
  6. ... influence a person's risk of developing these diseases. A large number of genetic and lifestyle factors, many of which remain unknown, likely determine the risk of developing ... Goth L, Eaton JW. Hereditary catalase deficiencies and increased risk of diabetes. Lancet. 2000 Nov ...
  7. ... person's risk of cardiovascular disease. All these factors cause the signs and symptoms of Tangier disease. ... Tangier disease ...
  8. ... Disorders (NORD) ACATALASEMIA ... P, Pay A. Catalase enzyme mutations and their association with diseases. Mol Diagn. 2004;8(3):141-9. doi: ...
  9. ... RV, Chandy M, Srivastava A. Molecular genetics of hereditary prothrombin ... >A testing): a disease-specific supplement to the standards and guidelines for ...
  10. ... increase the risk of cardiovascular disease. All these factors cause the signs and symptoms of Tangier disease. More About This Health ... E. The ABCA subfamily--gene and protein structures, functions and associated hereditary diseases. Pflugers Arch. 2007 Feb;453(5):581- ...
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