Hereditary factor II deficiency

Preferred Label : Hereditary factor II deficiency;

ICD-11 definition : Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms. Factor II deficiency is the most rare coagulation factor deficiency.;

ICD-11 synonym : Prothrombin deficiency;

ICD-11 inclusion : deficiency of factor 2; hereditary factor II deficiency disease; congenital factor II deficiency;

Details

Origin ID

1522212461;

Automatic exact mappings (from CISMeF team)
- Factor II deficiency [MedDRA Preferred Term]
- Factor II deficiency (disorder) [SNOMED CT concept]
- Hereditary Factor II Deficiency [NCIt concept]
- Hereditary factor II deficiency disease (disorder) [SNOMED CT concept]
- Prothrombin deficiency [MedDRA LLT]
- factor II deficiency [Blood Transfusion thesaurus concept]
- hypoprothrombinemias [MeSH Descriptor]
- prothrombin deficiency [DO Concept]
Currated CISMeF NLP mapping
- Congenital factor II deficiency [ORDO Disease]

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