Acquired hemophilia
MONDO:0019139Acquired hemophilia is a bleeding disorder that interferes with the body's blood clotting process. Signs and symptoms include prolonged bleeding, frequent nosebleeds, bruising throughout the body, solid swellings of congealed blood (hematomas), hematuria, and gastrointestinal or urologic bleeding. Acquired hemophilia occurs when the body's immune system attacks and disables a certain protein that helps the blood clot. About half of the cases are associated with other conditions, such as pregnancy, autoimmune disease, cancer, skin diseases, or allergic reactions to medications.
Also known as: acquired hemophilia, hemophilia, acquired
20 clinical trials for this condition and its sub-types, 2 tagged with Acquired hemophilia itself.
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Sub-types of Acquired hemophilia
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Acquired hemophilia A 6 trials
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Acquired factor XI deficiency 0 trials
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Acquired hemophilia B 0 trials