Haemophilia C - CISMeF

ICD-11 code : 3B13;

Preferred Label : Haemophilia C;

ICD-11 definition : A disease caused by genetically inherited mutations. This disease is characterised by decreased levels of factor XI leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding, easy bruising or, bleeding gums. Confirmation is by identification of mutation through genetic testing.;

ICD-11 synonym : Rosenthal factor deficiency; thromboplastin antecedent deficiency; hereditary factor XI deficiency disease; Rosenthal syndrome; congenital factor XI deficiency disease; factor XI deficiency; PTA deficiency; PTA - [plasma thromboplastin antecedent] deficiency; congenital factor XI deficiency; Rosenthal disease; plasma thromboplastin antecedent deficiency;

Details

Origin ID

413739466;

Automatic exact mappings (from CISMeF team)
- Factor XI deficiency (disorder) [SNOMED CT concept]
- Haemophilia [MedDRA Preferred Term]
- Haemophilia [HPMULTI term]
- Hemi-neglect (finding) [SNOMED CT concept]
- Hemophilia [MedDRA LLT]
- Hemophilia [NCIt concept]
- Hemophilia [ORDO Disease]
- Hemophilia [PASCAL descriptor]
- Hemophilia (disorder) [SNOMED CT concept]
- factor XI deficiency [DO Concept]
- hemophilia [MedlinePlus Topic]
- hemophilia, nos [SNOMED Notion]
- purpura - coagulation defect [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Congenital factor XI deficiency [ICD-9 code]
- Congenital factor XI deficiency [ORDO Disease]
- Congenital factor XI deficiency [MedDRA LLT]
- Factor XI Deficiency [NCIt concept]
- Factor XI deficiency [OMIM Phenotype]
- Factor XI deficiency [MedDRA Preferred Term]
- Hereditary Factor XI Deficiency [NCIt concept]
- Hereditary factor XI deficiency [ICD-10 Sub-category]
- Hereditary factor XI deficiency disease (disorder) [SNOMED CT concept]
- Reduced factor XI activity [HPO term]
- factor XI deficiency [MeSH concept]
- factor xi deficiency [MeSH Descriptor]
- factor xi deficiency [Blood Transfusion thesaurus concept]
- hereditary factor xi deficiency disease [SNOMED Notion]
ICD-10 Mapping
- Hereditary factor XI deficiency [ICD-10 Sub-category]

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