Disease-gene associations mined from literature

Human genes for acquired von Willebrand syndrome

Acquired von Willebrand syndrome [DOID:0111146]

A blood coagulation disease characterized by development of a defect in clotting in the absence of previous bleeding symptoms, negative familial history, and occurrence in a relatively older age. Typically this develops secondarily to other disorders, such as lymphoproliferative, myeloproliferative, cardiovascular and autoimmune disorders.

Synonyms:  acquired von Willebrand syndrome,  DOID:0111146,  acquired von Willebrand disease,  acquired von Willebrand disorder,  acquired von Willebrand syndromes ...