Hereditary factor VIII deficiency

ICD-11 code : 3B10;

Preferred Label : Hereditary factor VIII deficiency;

ICD-11 definition : A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing.;

ICD-11 inclusion : Deficiency factor VIII with functional defect; functional factor VIII deficiency; Factor VIII deficiency NOS;

ICD-11 "other" category code : 3B10.Y;

ICD-11 "unspecified" category code : 3B10.Z;

Détails

Origin ID

1573164739;

UMLS CUI

C0019069;

Currated CISMeF NLP mapping
- Hemophilia A [NCIt concept]
- Hereditary factor VIII deficiency [ICD-10 category]
- Hereditary factor VIII deficiency disease (disorder) [SNOMED CT concept]
ICD-10 Mapping
- Hereditary factor VIII deficiency [ICD-10 category]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital factor VIII disorder [ICD-9 code]
- Congenital factor VIII disorder [MedDRA LLT]
- Haemophilia A [MedDRA LLT]
- Haemophilia A (Factor VIII) [MedDRA LLT]
- Hemophilia A [MedDRA LLT]
- Hemophilia A [NCIt concept]
- Hemophilia A (Factor VIII) [MedDRA LLT]
- Hemophilia a [OMIM Phenotype]
- Hereditary factor VIII deficiency [ICD-10 category]
- Hereditary factor VIII deficiency disease (disorder) [SNOMED CT concept]
- factor VIII deficiency [DO Concept]
- hemophilia A [MeSH Descriptor]
- hemophilia A [MeSH concept]
- hemophilia a, nos [SNOMED Notion]

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

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