hemophilia B - CISMeF

Preferred Label : hemophilia B;

CISMeF synonym : B, Haemophilia; Bs, Haemophilia;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0004363;

UMLS CUI

C0008533;

Automatic exact mappings (from CISMeF team)
- coagulation factor IX [ORDO Gene]
- coagulation factor IX [HGNC gene]
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 [MedDRA LLT]
- Haemophilia B (Factor IX) [MedDRA LLT]
- Hemophilia B [PASCAL descriptor]
- Hemophilia B [MedDRA LLT]
- 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-10 category (who)]
- Hereditary factor IX deficiency disease (disorder) [SNOMED CT concept]
- hemophilia [MedlinePlus Topic]
- hemophilia B [DO Concept]
- hemophilia B [Disease (Nov.)]
- hemophilia B [Blood Transfusion thesaurus concept]
- hemophilia b, nos [SNOMED Notion]
Related record
- hemophilia B [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 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]
- Factor IX deficiency (disorder) [SNOMED CT concept]
- Haemophilia B [ICD-11 Subcategory]
- Haemophilia B [MedDRA LLT]
- Haemophilia B (Factor IX) [MedDRA LLT]
- Hemophilia B [ORDO Disease]
- Hemophilia B [PASCAL descriptor]
- Hemophilia B [MedDRA LLT]
- Hemophilia B [NCIt concept]
- 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, nos [SNOMED Notion]
Validated automatic mappings to NTBT
- Hereditary factor IX deficiency [ICD-11 Category]

Keyword's position in hierarchy(ies) :

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