Concept information
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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
Preferred term
von Willebrand Disease, Type 1
Type
-
mesh:Descriptor
Definition
- A subtype of von Willebrand disease that results from a partial deficiency of VON WILLEBRAND FACTOR.
Broader concept
Entry terms
- Type 1 von Willebrand Disease
- Type I von Willebrand Disease
- von Willebrand Disease, Type I
Allowable Qualifier(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)
In other languages
-
French
-
Maladie de von Willebrand de type I
URI
http://data.loterre.fr/ark:/67375/JVR-K08K8SPQ-J
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