Acquired hemophilia A
MONDO:0035735An acquired form of hemophilia A, resulting in spontaneous bleeding in individuals with no history of bleeding disorders. It is believed to be caused by spontaneous inhibition of clotting factor VIII by autoantibodies, and is usually associated with other autoimmune conditions.
Also known as: AHA
18 clinical trials for this condition and its sub-types, 6 tagged with Acquired hemophilia A itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of