Hereditary thrombophilia

ICD-11 code : 3B61.0;

Preferred Label : Hereditary thrombophilia;

ICD-11 definition : A disease caused by determinants arising after birth or genetically inherited factors leading to abnormalities in blood. This disease is characterised by abnormality of blood coagulation that increases the risk of thrombosis, clots in blood vessels. This disease may present with deep vein thrombosis or pulmonary embolism. Confirmation is identification of abnormal blood coagulation in a blood sample.;

ICD-11 synonym : Primary thrombophilia; factor V Leiden thrombophilia;

ICD-11 inclusion : Factor V Leiden; Prothrombin gene mutation; Factor V defects; heparin co-factor II deficiency; antithrombin deficiency; Hereditary thrombotic disorders;

ICD-11 "other" category code : 3B61.0Y;

Details

Origin ID

535489185;

UMLS CUI

C2584620;

Automatic exact mappings (from CISMeF team)
- Factor V Leiden thrombophilia [MedDRA LLT]
- thrombophilia due to activated protein C resistance [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Hereditary thrombophilia (disorder) [SNOMED CT concept]
- Thrombophilia, hereditary [MeSH concept]
- thrombophilia, hereditary [MeSH Supplementary Concept]
ICD-10 Mapping
- Primary thrombophilia [ICD-10 Sub-category]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary thrombophilia (disorder) [SNOMED CT concept]
- Primary thrombophilia [ICD-10 Sub-category]
- Rare hereditary thrombophilia [ORDO Disease]
- Thrombophilia, hereditary [MeSH concept]
- thrombophilia, hereditary [MeSH Supplementary Concept]
Validated automatic mappings to BTNT
- Rare hereditary thrombophilia [ORDO Disease]
Validated automatic mappings to NTBT
- Primary thrombophilia [ICD-10 Sub-category]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients