Haemophilia A - CISMeF

ICD-11 code : 3B10.0;

Preferred Label : Haemophilia A;

ICD-11 definition : Haemophilia A is the most common form of haemophilia characterised by spontaneous or prolonged haemorrhages due to factor VIII deficiency. Depending on the extent of the factor VIII deficiency, it can be severe (biological activity of factor VIII below 1%), moderately severe (activity of factor VIII between 1% and 5%), or mild (activity of factor VIII between 5 and 40%).;

ICD-11 synonym : congenital factor VIII disorder; hereditary haemophilia; AHG - [antihaemophilic globulin] deficiency disease; classic haemophilia; antihaemophilic globulin deficiency; haemophilia; familial haemophilia; AHG deficiency; sex-linked factor VIII deficiency; AHG deficiency disease; AHG - [antihaemophilic globulin] deficiency; subhaemophilia;

ICD-11 inclusion : Haemophilia NOS;

Détails

Origin ID

337607970;

Automatic exact mappings (from CISMeF team)
- Coagulation factor VIII [LOINC component]
- Congenital factor VIII disorder [ICD-9 code]
- Congenital factor VIII disorder [MedDRA LLT]
- Hemophilia - specialty (qualifier value) [SNOMED CT concept]
- factor VIII deficiency [DO Concept]
- haemophilia [EMDN type]
- purpura - coagulation defect [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Factor VIII deficiency [OMIM Phenotype]
- Haemophilia [MedDRA Preferred Term]
- Haemophilia [HPMULTI term]
- Haemophilia A [MedDRA LLT]
- Hemophilia [MedDRA LLT]
- Hemophilia [NCIt concept]
- Hemophilia [ORDO Disease]
- Hemophilia [PASCAL descriptor]
- Hemophilia (disorder) [SNOMED CT concept]
- Hemophilia A [NCIt concept]
- Hemophilia A [MedDRA LLT]
- Hemophilia A [PASCAL descriptor]
- Hemophilia A [ORDO Disease]
- Hemophilia a [OMIM Phenotype]
- Hereditary factor VIII deficiency disease (disorder) [SNOMED CT concept]
- Reduced factor VIII activity [HPO term]
- haemophilia [Blood Transfusion thesaurus concept]
- hemophilia [MedlinePlus Topic]
- hemophilia A [MeSH Descriptor]
- hemophilia A [MeSH concept]
- hemophilia a, nos [SNOMED Notion]
- hemophilia, nos [SNOMED Notion]
ICD-10 Mapping
- Hereditary factor VIII deficiency [ICD-10 category]

Position du mot-clé dans l'(les) arborescence(s) :

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