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