von Willebrand Diseases D014842

Related MeSH Hierarchy (5)

Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Blood Platelet Disorders » von Willebrand Diseases

Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Hemorrhagic Disorders » von Willebrand Diseases

Description

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.   MeSH

Subtype Terms (3)


Phase 2 Indicated Drugs (3)

Phase 1 Indicated Drugs (1)

Other Experimental Indicated Drugs (5)


Organization Involved with Phase 1 Indications (1)

Organization Involved with Other Experimental Indications (3)

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UMLS Data


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