Von Willebrand's disease

Preferred Label : Von Willebrand's disease;

Inclusion CIM-10 : Angiohemophilia; Factor VIII deficiency with vascular defect; Vascular hemophilia;

ICD-10 exclusion note : factor VIII deficiency NOS (D66); factor VIII deficiency with functional defect (D66); capillary fragility (hereditary) (D69.8);

Diag associé à un acte (%) : 35.3;

Source : OMS;

Date de début : 01/01/1997;

Détails

Origin ID

D680;

UMLS CUI

C0042974;

Currated CISMeF NLP mapping
- Von Willebrand disease [ORDO Disease]
- Von Willebrand disease [ICD-11 Category]
- Von Willebrand's disease [MedDRA Preferred Term]
- Von Willebrand's disease [ICD-9 code]
- Von Willebrands disease [ICD-10 Sub-category (who)]
- Willebrand disease [PASCAL descriptor]
- von Willebrand Disease [NCIt concept]
- 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 [MeSH Supplementary Concept]
- von willebrand disease, platelet type [SNOMED Notion]
- von willebrand diseases [MeSH concept]
- von willebrand diseases [MeSH Descriptor]
DO Cross reference
- von Willebrand's disease [DO Concept]
Excluded by
- Hereditary factor VIII deficiency [ICD-10 category]
- Qualitative platelet defects [ICD-10 Sub-category]
ICD-10 exclusion(s)
- Hereditary factor VIII deficiency [ICD-10 category]
- Other specified hemorrhagic conditions [ICD-10 Sub-category]
Orphanet concepts
- Von Willebrand disease [ORDO Disease]
- Von Willebrand disease type 1 [ORDO Disease]
- Von Willebrand disease type 2 [ORDO Disease]
- Von Willebrand disease type 2A [ORDO Disease]
- Von Willebrand disease type 2B [ORDO Disease]
- Von Willebrand disease type 2M [ORDO Disease]
- Von Willebrand disease type 2N [ORDO Disease]
- Von Willebrand disease type 3 [ORDO Disease]
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 [MedDRA Preferred Term]
- Von Willebrand's disease [ICD-9 code]
- Von Willebrand's factor deficiency [MedDRA LLT]
- von Willebrand Disease [NCIt concept]
- 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 Descriptor]
- von willebrand diseases [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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