Hereditary factor IX deficiency

Preferred Label : Hereditary factor IX deficiency;

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

Diag associé à un acte (%) : 28;

Details

Origin ID

D67;

Automatic exact mappings (from CISMeF team)
- Coagulation defect [ICPC-3 diagnosis]
- Hemophilia B without inhibitors [MedDRA LLT]
- Other specified or unknown blood, blood-forming organs, immune system diagnoses or diseases [ICPC-3 diagnosis]
Currated CISMeF NLP mapping
- Christmas disease (Factor IX) [MedDRA LLT]
- Congenital factor IX disorder [ICD-9 code]
- Congenital factor IX disorder [MedDRA LLT]
- Factor IX deficiency [MedDRA Preferred Term]
- Haemophilia B [ICD-11 Subcategory]
- Haemophilia B (Factor IX) [MedDRA LLT]
- Hemophilia B [PASCAL descriptor]
- Hemophilia B [NCIt concept]
- Hemophilia B [ORDO Disease]
- Hemophilia B (Factor IX) [MedDRA LLT]
- Hemophilia b [OMIM Phenotype]
- Hereditary factor IX deficiency [ICD-10 category]
- Hereditary factor IX deficiency [ICD-11 Category]
- Hereditary factor IX deficiency disease (disorder) [SNOMED CT concept]
- hemophilia B [DO Concept]
- hemophilia B [Disease (Nov.)]
- hemophilia B [MeSH Descriptor]
- hemophilia B [MeSH concept]
- hemophilia b, nos [SNOMED Notion]
Exclusion(s) CIM-10
- Abnormal findings on examination of blood, without diagnosis [ICD-10 Block (who)]
HRDO close match(es)
- Hemophilia [ORDO Disease]
Manual BTNT mappings - CISMeF
- Bleeding disorder in hemophilia B carriers [ORDO Disease]
- Mild hemophilia B [ORDO Disease]
- Moderate hemophilia B [ORDO Disease]
- Severe hemophilia B [ORDO Disease]
Metaterm(s)
- hematology [CISMeF Metaterm]
SNOMED int. exact match(es)
- hemophilia b, nos [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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