von willebrand disease, nos - CISMeF

CISMeF

chu

Von willebrand disease, nosSNOMED Notion

Preferred Label : von willebrand disease, nos;

Détails

Origin ID

DC-64100;

UMLS CUI

C0042974;

Automatic exact mappings (from CISMeF team)
- Angiohaemophilia [MedDRA LLT]
- Angiohemophilia [MedDRA LLT]
- Hereditary von Willebrand disease type 1B (disorder) [SNOMED CT concept]
- Rare hemorrhagic disorder due to a constitutional platelet anomaly [ORDO Disease]
- Vascular haemophilia [MedDRA LLT]
- Vascular hemophilia [MedDRA LLT]
- 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 [NCIt concept]
- von Willebrand disease [Disease (Nov.)]
- von Willebrand disorder (disorder) [SNOMED CT concept]
- von Willebrand's disease [DO Concept]
- von willebrand disease, platelet type [MeSH Supplementary Concept]
- von willebrand diseases [MeSH Descriptor]
- von willebrand diseases [MeSH concept]
ICD-10 exact mapping(s)
- Von Willebrands disease [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Alpha delta granule deficiency [ORDO Disease]
- Autosomal dominant macrothrombocytopenia [ORDO Disease]
- Autosomal thrombocytopenia with normal platelets [ORDO Disease]
- Bleeding diathesis due to a collagen receptor defect [ORDO Disease]
- Bleeding disorder due to P2Y12 defect [ORDO Disease]
- Congenital amegakaryocytic thrombocytopenia [ORDO Disease]
- Familial platelet disorder with associated myeloid malignancy [ORDO Disease]
- Familial thrombocytosis [ORDO Disease]
- Fetal and neonatal alloimmune thrombocytopenia [ORDO Disease]
- MYH9-related disease [ORDO Disease]
- Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome [ORDO Disease]
- Scott syndrome [ORDO Disease]
- Stormorken-Sjaastad-Langslet syndrome [ORDO Disease]
- Thrombocytopenia-absent radius syndrome [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Rare coagulation disorder [ORDO Disease]
- Rare genetic coagulation disorder [ORDO Disease]
- Rare hemorrhagic disorder due to a constitutional coagulation factors defect [ORDO Disease]
Metaterm(s)
- hematology [CISMeF Metaterm]
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 [NCIt concept]
- von Willebrand disease [Disease (Nov.)]
- von Willebrand disorder (disorder) [SNOMED CT concept]
- von Willebrand's disease [DO Concept]
- von willebrand diseases [MeSH Descriptor]
- von willebrand diseases [MeSH concept]

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29/07/2025

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