Concept information
...
Hematologic Diseases
Blood Coagulation Disorders
Coagulation Protein Disorders
von Willebrand Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
von Willebrand Diseases
Terme préférentiel
von Willebrand Disease, Type 3
Type
-
mesh:Descriptor
Définition
- A subtype of von Willebrand disease that results from a total or near total deficiency of VON WILLEBRAND FACTOR.
Concept générique
Synonyme(s)
- Type 3 Von Willebrand's Disease
- Type 3 VWD
- Von Willebrand Disease, Severe Form
Qualificatif(s) autorisé(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
Traductions
-
français
-
Forme grave de la maladie de von Willebrand
-
Forme sévère de la maladie de von Willebrand
-
Maladie de von Willebrand de type III
URI
http://data.loterre.fr/ark:/67375/JVR-D2LCMFXH-3
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