Hereditary factor IX deficiency

Preferred Label : Hereditary factor IX deficiency;

Inclusion CIM-10 : Plasma thromboplastin component [PTC] deficiency; Christmas disease; Hemophilia B; Factor IX deficiency (with functional defect);

Diag associé à un acte (%) : 28.3;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D67;

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 (Factor IX) [MedDRA LLT]
- Hemophilia B [PASCAL descriptor]
- Hemophilia B [ORDO Disease]
- Hemophilia B [NCIt concept]
- Hemophilia B [MedDRA LLT]
- Hemophilia B (Factor IX) [MedDRA LLT]
- Hemophilia b [OMIM Phenotype]
- Hereditary factor IX deficiency [ICD-11 Category]
- Hereditary factor IX deficiency [ICD-10 category (who)]
- Hereditary factor IX deficiency disease (disorder) [SNOMED CT concept]
- hemophilia [MedlinePlus Topic]
- hemophilia B [MeSH concept]
- hemophilia B [DO Concept]
- hemophilia B [MeSH Descriptor]
- hemophilia B [Disease (Nov.)]
- hemophilia B [Blood Transfusion thesaurus concept]
- hemophilia b, nos [SNOMED Notion]
DO Cross reference
- hemophilia B [DO Concept]
Manual NTBT 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]
Orphanet concepts
- Bleeding disorder in hemophilia B carriers [ORDO Disease]
- Hemophilia B [ORDO Disease]
- Mild hemophilia B [ORDO Disease]
- Moderate hemophilia B [ORDO Disease]
- Severe hemophilia B [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 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]
- Factor IX deficiency (disorder) [SNOMED CT concept]
- Haemophilia B [ICD-11 Subcategory]
- 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-11 Category]
- 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]

Keyword's position in hierarchy(ies) :

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