hemophilia a, nos

Preferred Label : hemophilia a, nos;

Détails

Origin ID

DC-63120;

UMLS CUI

C0019069;

Currated CISMeF NLP mapping
- Factor VIII deficiency [OMIM Phenotype]
- Haemophilia [MedDRA Preferred Term]
- Haemophilia A [ICD-11 Subcategory]
- Haemophilia A [MedDRA LLT]
- Haemophilia NOS [MedDRA LLT]
- Hemophilia [NCIt concept]
- Hemophilia [PASCAL descriptor]
- Hemophilia [ORDO Disease]
- Hemophilia [MedDRA LLT]
- Hemophilia (disorder) [SNOMED CT concept]
- Hemophilia A [PASCAL descriptor]
- Hemophilia A [NCIt concept]
- Hemophilia A [ORDO Disease]
- Hemophilia A [MedDRA LLT]
- Hemophilia A (Factor VIII) [MedDRA LLT]
- Hemophilia a [OMIM Phenotype]
- Hereditary factor VIII deficiency [ICD-10 category]
- Hereditary factor VIII deficiency [ICD-10 category (who)]
- Hereditary factor VIII deficiency disease (disorder) [SNOMED CT concept]
- Reduced factor VIII activity [HPO term]
- factor VIII deficiency [MeSH concept]
- hemophilia [MedlinePlus Topic]
- hemophilia A [Disease (Nov.)]
- hemophilia A [MeSH Descriptor]
- hemophilia A [MeSH concept]
- hemophilia A [Blood Transfusion thesaurus concept]
- hemophilia B [MeSH Descriptor]
ICD-10 exact mapping(s)
- Hereditary factor VIII deficiency [ICD-10 category (who)]
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 CT concept
- Hereditary factor VIII deficiency disease (disorder) [SNOMED CT concept]
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 [NCIt concept]
- Hemophilia A (Factor VIII) [MedDRA LLT]
- Hemophilia a [OMIM Phenotype]
- Hereditary factor VIII deficiency [ICD-10 category]
- Hereditary factor VIII deficiency [ICD-11 Category]
- Hereditary factor VIII deficiency [ICD-10 category (who)]
- Hereditary factor VIII deficiency disease (disorder) [SNOMED CT concept]
- factor VIII deficiency [DO Concept]
- hemophilia A [MeSH Descriptor]
- hemophilia A [MeSH concept]
Validated automatic mappings to NTBT
- hemophilia [Disease (Nov.)]

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