... C3 inactivator deficiency Complement component 3 inactivator deficiency Hereditary factor I deficiency disease Genetic Testing Registry: Hereditary factor I deficiency disease ...

... Testing Registry: Hemophilia b(m) Genetic Testing Registry: Hereditary factor IX deficiency disease Genetic Testing Registry: Hereditary factor VIII deficiency disease ...

... Rosenthal syndrome Rosenthal's disease Genetic Testing Registry: Hereditary factor XI deficiency disease Congenital factor XI deficiency National Organization for Rare ...

... the condition. Afibrinogenemia Familial afibrinogenemia Genetic Testing Registry: Hereditary factor I deficiency disease Familial afibrinogenemia National Organization for Rare Disorders (NORD) ...

Factor V deficiency is a rare bleeding disorder. The signs and symptoms of this condition can begin at any age, although the most severe cases are apparent ...

... person's risk of cardiovascular disease. All these factors cause the signs and symptoms of Tangier disease. ... Tangier disease ...

... Disorders (NORD) ACATALASEMIA ... P, Pay A. Catalase enzyme mutations and their association with diseases. Mol Diagn. 2004;8(3):141-9. doi: ...

... s own cells. It is likely that other factors, both genetic and environmental, play a role in the variability of the signs and ... occurrence of invasive infection, atherosclerosis, and rheumatic disease. Medicine (Baltimore). 2005 Jan;84(1):23-34. ...

... Acute porphyrias include acute intermittent porphyria and ALAD deficiency ... the disease never experience signs or symptoms.Acute intermittent porphyria ...

... purpura. In people with reduced ADAMTS13 enzyme activity, factors such as pregnancy, surgery, and infection may trigger ... on PubMed Tsai HM. Is severe deficiency of ADAMTS-13 specific for thrombotic thrombocytopenic purpura? ...