hemophilia b, nos

Preferred Label : hemophilia b, nos;

Origin ID

DC-63160;

UMLS CUI

C0008533;

ICD-10 exact mapping(s)
- Hereditary factor IX deficiency [ICD-10 category (who)]
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 CT concept
- Hereditary factor IX deficiency disease (disorder) [SNOMED CT concept]
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 [MeSH Descriptor]
- hemophilia B [MeSH concept]
- hemophilia B [Disease (Nov.)]
- hemophilia B [DO Concept]
Validated automatic mappings to NTBT
- Hereditary factor IX deficiency [ICD-11 Category]