von Willebrand Disease

Preferred Label : von Willebrand Disease;

NCIt related terms : von Willebrand Disorder; Von Willebrand's disease;

NCIt definition : Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von Willebrand factor. The latter plays an important role in platelet adhesion. Signs and symptoms include bruises, nose bleeding, gum bleeding following a dental procedure, heavy menstrual bleeding, and gastrointestinal bleeding.;

Alternative definition : NICHD: Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von Willebrand factor. The latter plays an important role in platelet adhesion. Signs and symptoms include mucocutaneous bleeding.;

Codes from synonyms : D68.0;

Details

Origin ID

C68677;

UMLS CUI

C0042974;

Automatic exact mappings (from CISMeF team)
- Encephalitis lethargica (disorder) [SNOMED CT concept]
- Glycogen storage disease, type I (disorder) [SNOMED CT concept]
- Hereditary von Willebrand disease type 1B (disorder) [SNOMED CT concept]
- Von Gierke's disease [MedDRA LLT]
- glycogen storage disease type i [MeSH Descriptor]
- neurofibromatosis [MedlinePlus Topic]
- neurofibromatosis 1 [MeSH Descriptor]
- platelet disorders [MedlinePlus Topic]
- purpura - coagulation defect [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Von Willebrand disease [ICD-11 Category]
- Von Willebrand disease [ORDO Disease]
- Von Willebrand's disease [ICD-10 Sub-category]
- Von Willebrand's disease [ICD-9 code]
- Von Willebrand's disease [MedDRA Preferred Term]
- Von Willebrands disease [ICD-10 Sub-category (who)]
- Willebrand disease [PASCAL descriptor]
- von Willebrand disease [Disease (Nov.)]
- von Willebrand disorder (disorder) [SNOMED CT concept]
- von Willebrand's disease [DO Concept]
- von willebrand disease, nos [SNOMED Notion]
- von willebrand disease, platelet type [SNOMED Notion]
- von willebrand disease, platelet type [MeSH Supplementary Concept]
- von willebrand diseases [MeSH Descriptor]
- von willebrand diseases [MeSH concept]
DO Cross reference
- von Willebrand's disease [DO Concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Angiohaemophilia [MedDRA LLT]
- Angiohemophilia [MedDRA LLT]
- Factor VIII Rag deficiency [MedDRA LLT]
- Pseudohaemophilia [MedDRA LLT]
- Pseudohemophilia [MedDRA LLT]
- Vascular haemophilia [MedDRA LLT]
- Vascular hemophilia [MedDRA LLT]
- Von Willebrand disease [ORDO Disease]
- Von Willebrand disease [ICD-11 Category]
- Von Willebrand's disease [ICD-9 code]
- Von Willebrand's disease [MedDRA Preferred Term]
- Von Willebrand's disease [ICD-10 Sub-category]
- Von Willebrand's factor deficiency [MedDRA LLT]
- Von Willebrands disease [ICD-10 Sub-category (who)]
- von Willebrand disease [Disease (Nov.)]
- von Willebrand disorder (disorder) [SNOMED CT concept]
- von Willebrand's disease [DO Concept]
- von willebrand disease, nos [SNOMED Notion]
- von willebrand diseases [MeSH concept]
- von willebrand diseases [MeSH Descriptor]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
- mCode Elixhauser Coagulation Deficiency Value Set [NCIt concept]
- mCode Terminology [NCIt concept]
disease_has_normal_cell_origin
- Hematopoietic and Lymphoid Cell [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic and Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Hematopoietic and Lymphatic System [NCIt concept]
pathogenesis_of_disease_involves_gene
- VWF Gene [NCIt concept]
- VWF wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients