| Descriptor English: | von Willebrand Diseases | ||||||
| Descriptor Spanish: |
Enfermedades de von Willebrand
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| Descriptor Portuguese: | Doenças de von Willebrand | ||||||
| Descriptor French: | Maladies de von Willebrand | ||||||
| Entry term(s): |
Angiohemophilia Angiohemophilias Disorder, Von Willebrand Hemophilia, Vascular Pseudohemophilia, Vascular Pseudohemophilias, Vascular Vascular Hemophilia Vascular Hemophilias Vascular Pseudohemophilia Vascular Pseudohemophilias Von Willebrand Disorder Von Willebrand's Factor Deficiency von Willebrand Disease von Willebrand Disease, Recessive Form von Willebrand's Disease von Willebrand's Diseases |
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| Tree number(s): |
C15.378.100.100.900 C15.378.100.141.900 C15.378.140.900 C15.378.463.920 C16.320.099.920 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D014842 | ||||||
| Scope note: | 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. |
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| Annotation: | note specific types of Von Willebrand Disease are available |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 2010; see VON WILLEBRAND DISEASE 1999-2009; see VON WILLEBRAND'S DISEASE 1968-1998, see HEMORRHAGIC DIATHESIS 1967, see THROMBOCYTOPATHY 1963-1966 |
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| History Note: | 2010(1963) |
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| DeCS ID: | 15243 | ||||||
| Unique ID: | D014842 | ||||||
| NLM Classification: | WH 312 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1968/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2013/07/08 |
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von Willebrand Diseases
- Preferred
von Willebrand Disease, Recessive Form
- Narrower
| Concept UI |
M0022853 |
| Scope note | 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. |
| Preferred term | von Willebrand Diseases |
| Entry term(s) |
Angiohemophilia Angiohemophilias Disorder, Von Willebrand Hemophilia, Vascular Pseudohemophilia, Vascular Pseudohemophilias, Vascular Vascular Hemophilia Vascular Hemophilias Vascular Pseudohemophilia Vascular Pseudohemophilias Von Willebrand Disorder Von Willebrand's Factor Deficiency von Willebrand Disease von Willebrand's Disease von Willebrand's Diseases |
| Concept UI |
M0533280 |
| Preferred term | von Willebrand Disease, Recessive Form |
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