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
Terme préférentiel
von Willebrand Disease, Type 1
Type
-
mesh:Descriptor
Définition
- A subtype of von Willebrand disease that results from a partial deficiency of VON WILLEBRAND FACTOR.
Concept générique
Synonyme(s)
- Type 1 von Willebrand Disease
- Type I von Willebrand Disease
- von Willebrand Disease, Type I
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
-
Maladie de von Willebrand de type I
URI
http://data.loterre.fr/ark:/67375/JVR-K08K8SPQ-J
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