Haemophilia B - CISMeF

ICD-11 code : 3B11.0;

Preferred Label : Haemophilia B;

ICD-11 definition : Haemophilia B is a form of haemophilia characterised by spontaneous or prolonged haemorrhages due to factor IX deficiency. Depending on the extent of the factor IX deficiency, it can be severe (biological activity of factor IX below 1%), moderately severe (activity of factor IX between 1% and 5%), or mild (activity of factor IX between 5 and 40%).;

ICD-11 synonym : Symptomatic form of haemophilia B in female carriers; Severe haemophilia B; Moderately severe haemophilia B; PTC - [plasma thromboplastin component] deficiency; Mild haemophilia B; deficiency of functional factor ix; plasma thromboplastin component deficiency;

ICD-11 inclusion : PTC - [plasma thromboplastin component] deficiency; Symptomatic form of haemophilia B in female carriers; Severe haemophilia B; Moderately severe haemophilia B; Mild haemophilia B;

Details

Origin ID

1901375668;

UMLS CUI

C0008533;

Automatic exact mappings (from CISMeF team)
- coagulation factor IX [HGNC gene]
Currated CISMeF NLP mapping
- Christmas disease (Factor IX) [MedDRA LLT]
- Congenital factor IX disorder [MedDRA LLT]
- Congenital factor IX disorder [ICD-9 code]
- Factor IX deficiency [MedDRA Preferred Term]
- Haemophilia B [MedDRA LLT]
- Haemophilia B (Factor IX) [MedDRA LLT]
- Hemophilia B [NCIt concept]
- Hemophilia B [PASCAL descriptor]
- Hemophilia B [ORDO Disease]
- Hemophilia B [MedDRA LLT]
- 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 B [MeSH Descriptor]
- hemophilia B [MeSH concept]
- hemophilia B [DO Concept]
- hemophilia B [Disease (Nov.)]
- hemophilia b, nos [SNOMED Notion]
ICD-10 Mapping
- Hereditary factor IX deficiency [ICD-10 category]
See also inter- (CISMeF)
- Congenital factor XI deficiency [ORDO Disease]
- coagulation factor IX [ORDO Gene]
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 [MedDRA LLT]
- Haemophilia B (Factor IX) [MedDRA LLT]
- Hemophilia B [NCIt concept]
- Hemophilia B [ORDO Disease]
- Hemophilia B [PASCAL descriptor]
- Hemophilia B [MedDRA LLT]
- Hemophilia B (Factor IX) [MedDRA LLT]
- Hemophilia b [OMIM Phenotype]
- Hereditary factor IX deficiency [ICD-10 category]
- Hereditary factor IX deficiency disease (disorder) [SNOMED CT concept]
- hemophilia B [DO Concept]
- hemophilia B [MeSH Descriptor]
- hemophilia B [MeSH concept]
- hemophilia B [Disease (Nov.)]
- hemophilia b, nos [SNOMED Notion]

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