von willebrand disease, type 2A

Preferred Label : von willebrand disease, type 2A;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0528879;

UMLS CUI

C1282968;

Automatic exact mappings (from CISMeF team)
- Von Willebrand disease type 2A [ICD-11 More detail]
Currated CISMeF NLP mapping
- Hereditary von Willebrand disease type 2A (disorder) [SNOMED CT concept]
- Von Willebrand disease type 2A [ORDO Disease]
- Von willebrand disease, type 2 [OMIM Phenotype]
- von Willebrand Disease, Type 2A [NCIt concept]
- von Willebrand disease type 2A (disorder) [SNOMED CT concept]
- von Willebrand disease, type IIA (disorder) [SNOMED CT concept]
- von willebrand disease, type iia [SNOMED Notion]
Related record
- von willebrand disease, type 2 [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary von Willebrand disease type 2A (disorder) [SNOMED CT concept]
- Von Willebrand disease type 2A [ORDO Disease]
- von Willebrand Disease, Type 2A [NCIt concept]
- von Willebrand disease type 2A (disorder) [SNOMED CT concept]
- von Willebrand disease, type IIA (disorder) [SNOMED CT concept]
- von willebrand disease, type iia [SNOMED Notion]