ICD-9-CM 286.4 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 286.4 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
Group of hemorrhagic disorders in which the von willebrand factor is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor viii, and impaired platelet adhesion
Hemophilioid disorder due to deficiency of von willebrand factor and thus of factor viii complex
Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von willebrand factor. The latter plays an important role in platelet adhesion. Signs and symptoms include bruises, nose bleeding, gum bleeding following a dental procedure, heavy menstrual bleeding, and gastrointestinal bleeding
Includes true von willebrand disease with mutation at the vwf locus, as well as mimicking disorders with other mutations (pseudo vwd) and acquired von willebrand syndrome