Hereditary factor VIII deficiency

Preferred Label : Hereditary factor VIII deficiency;

Inclusion CIM-10 : Classical hemophilia; Hemophilia A; Hemophilia NOS; Deficiency factor VIII (with functional defect);

ICD-10 exclusion note : factor VIII deficiency with vascular defect (D68.0);

Diag associé à un acte (%) : 46.8;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D66;

UMLS CUI

C0019069;

Automatic exact mappings (from CISMeF team)
- Hemophilia [LOINC component]
- Hemophilia - specialty (qualifier value) [SNOMED CT concept]
- coagulation factor VIII [ORDO Gene]
- coagulation factor VIII [HGNC gene]
- factor VIII deficiency [DO Concept]
Currated CISMeF NLP mapping
- Factor VIII deficiency [OMIM Phenotype]
- Haemophilia [MedDRA Preferred Term]
- Haemophilia A [MedDRA LLT]
- Haemophilia NOS [MedDRA LLT]
- Hemophilia [ORDO Disease]
- Hemophilia [MedDRA LLT]
- Hemophilia [NCIt concept]
- Hemophilia [PASCAL descriptor]
- Hemophilia (disorder) [SNOMED CT concept]
- Hemophilia A [NCIt concept]
- Hemophilia A [MedDRA LLT]
- Hemophilia A [ORDO Disease]
- Hemophilia A [PASCAL descriptor]
- Hemophilia a [OMIM Phenotype]
- Hereditary factor VIII deficiency [ICD-11 Category]
- Hereditary factor VIII deficiency disease (disorder) [SNOMED CT concept]
- factor VIII deficiency [MeSH concept]
- hemophilia [MedlinePlus Topic]
- hemophilia A [MeSH concept]
- hemophilia A [MeSH Descriptor]
- hemophilia A [Blood Transfusion thesaurus concept]
- hemophilia a, nos [SNOMED Notion]
- hemophilia, nos [SNOMED Notion]
DO Cross reference
- factor VIII deficiency [DO Concept]
Excluded by
- Von Willebrand's disease [ICD-10 Sub-category]
ICD-10 exclusion(s)
- Von Willebrand's disease [ICD-10 Sub-category]
Manual NTBT mappings (CISMeF)
- Bleeding disorder in hemophilia A carriers [ORDO Disease]
- Mild hemophilia A [ORDO Disease]
Metaterm(s)
- hematology [CISMeF Metaterm]
Orphanet concepts
- Bleeding disorder in hemophilia A carriers [ORDO Disease]
- Hemophilia A [ORDO Disease]
- Mild hemophilia A [ORDO Disease]
- Moderate hemophilia A [ORDO Disease]
- Severe hemophilia A [ORDO Disease]
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 [ICD-9 code]
- Congenital factor VIII disorder [MedDRA LLT]
- Factor VIII deficiency [MedDRA Preferred Term]
- Factor VIII deficiency [OMIM Phenotype]
- Factor VIII deficiency (disorder) [SNOMED CT concept]
- 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-11 Category]
- Hereditary factor VIII deficiency disease (disorder) [SNOMED CT concept]
- factor VIII deficiency [MeSH concept]
- factor VIII deficiency [DO 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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