Hereditary factor VIII deficiency

Preferred Label : Hereditary factor VIII deficiency;

Code considérée comme une complication de niveau 2, 3 ou 4 : 2;

Diag associé à un acte (%) : 46;

Details

Origin ID

D66;

Automatic exact mappings (from CISMeF team)
- Coagulation defect [ICPC-3 diagnosis]
- Hemophilia A without inhibitors [MedDRA LLT]
- Other specified or unknown blood, blood-forming organs, immune system diagnoses or diseases [ICPC-3 diagnosis]
Currated CISMeF NLP mapping
- Factor VIII deficiency [OMIM Phenotype]
- Factor VIII deficiency (disorder) [SNOMED CT concept]
- Haemophilia [MedDRA Preferred Term]
- Haemophilia A [MedDRA LLT]
- Haemophilia NOS [MedDRA LLT]
- Hemophilia [ORDO Disease]
- Hemophilia [MedDRA LLT]
- Hemophilia A [MedDRA LLT]
- Hemophilia A [ORDO Disease]
- Hemophilia A [PASCAL descriptor]
- Hemophilia A [NCIt concept]
- Hemophilia a [OMIM Phenotype]
- Reduced factor VIII activity [HPO term]
- factor VIII deficiency [MeSH concept]
- hemophilia [MedlinePlus Topic]
- hemophilia A [MeSH Descriptor]
- hemophilia A [MeSH concept]
- hemophilia a, nos [SNOMED Notion]
- hemophilia, nos [SNOMED Notion]
Exclusion(s) CIM-10
- Abnormal findings on examination of blood, without diagnosis [ICD-10 Block (who)]
- Von Willebrands disease [ICD-10 Sub-category (who)]
HRDO close match(es)
- Hemophilia [ORDO Disease]
Manual BTNT mappings - CISMeF
- Bleeding disorder in hemophilia A carriers [ORDO Disease]
- Mild hemophilia A [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Rare hemorrhagic disorder due to a constitutional coagulation factors defect [ORDO Disease]
Metaterm(s)
- hematology [CISMeF Metaterm]
SNOMED int. exact match(es)
- hemophilia a, nos [SNOMED Notion]
- hemophilia, nos [SNOMED Notion]
- mild hemophilia a [SNOMED Notion]
- moderate hemophilia a [SNOMED Notion]
- severe hemophilia a [SNOMED Notion]
See also inter- (CISMeF)
- hemophilia A [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital factor VIII disorder [MedDRA LLT]
- Congenital factor VIII disorder [ICD-9 code]
- Haemophilia A [MedDRA LLT]
- Haemophilia A (Factor VIII) [MedDRA LLT]
- Hemophilia A [MedDRA LLT]
- Hemophilia A [ORDO Disease]
- Hemophilia A [NCIt concept]
- Hemophilia A (Factor VIII) [MedDRA LLT]
- Hemophilia a [OMIM Phenotype]
- Hereditary factor VIII deficiency disease (disorder) [SNOMED CT concept]
- hemophilia A [MeSH Descriptor]
- hemophilia A [MeSH concept]
- hemophilia a, nos [SNOMED Notion]
Validated automatic mappings to NTBT
- hemophilia [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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