Related MeSH Hierarchy (5)
Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Blood Coagulation Disorders » Blood Coagulation Disorders, Inherited » von Willebrand Diseases
Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Blood Coagulation Disorders » Coagulation Protein Disorders » von Willebrand Diseases
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
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Blood Coagulation Disorders, Inherited » 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
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Subtype Terms (3)
von Willebrand Disease, Type 1
1 approved drug
von Willebrand Disease, Type 2
1 experimental drug
von Willebrand Disease, Type 3
1 approved drug
Approved Indicated Drugs (2)
Phase 4 Indicated Drugs (1)
Phase 3 Indicated Drugs (2)
Phase 2 Indicated Drugs (3)
Phase 1 Indicated Drugs (3)
Other Experimental Indicated Drugs (5)
Organization Involved with Phase 4 Indications (5)
Organization Involved with Phase 3 Indications (11)
Organization Involved with Phase 2 Indications (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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