tyrosinemia, type II

Preferred Label : tyrosinemia, type II;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0336267;

UMLS CUI

C0268487;

Automatic exact mappings (from CISMeF team)
- hypertyrosinemia, richner-hanhart type [SNOMED Notion]
Currated CISMeF NLP mapping
- Hypertyrosinemia, Richner-Hanhart type (disorder) [SNOMED CT concept]
- Tyrosinaemia type 2 [ICD-11 Sub-sub category]
- Tyrosinaemia type II [MedDRA LLT]
- Tyrosinemia Type II [NCIt concept]
- Tyrosinemia type 2 [ORDO Disease]
- Tyrosinemia type II [MedDRA LLT]
- Tyrosinemia, type II [OMIM Phenotype]
- tyrosinemia type II [DO Concept]
- tyrosinemia type II [Disease (Nov.)]
Related record
- tyrosinemias [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deficiency of tyrosine aminotransferase (disorder) [SNOMED CT concept]
- Hypertyrosinemia, Richner-Hanhart type (disorder) [SNOMED CT concept]
- Tyrosinaemia type 2 [ICD-11 Sub-sub category]
- Tyrosinaemia type II [MedDRA LLT]
- Tyrosinemia Type II [NCIt concept]
- Tyrosinemia type 2 [ORDO Disease]
- Tyrosinemia type II [MedDRA LLT]
- Tyrosinemia, type II [OMIM Phenotype]
- hypertyrosinemia, richner-hanhart type [SNOMED Notion]
- tyrosinemia type II [DO Concept]
- tyrosinemia type II [Disease (Nov.)]