tyrosinosis - CISMeF

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CISMeF

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TyrosinosisMeSH Supplementary Concept

Preferred Label : tyrosinosis;

MeSH note : distinct from tyrosinemia;

Details

Origin ID

C562659;

UMLS CUI

C0268484;

Automatic exact mappings (from CISMeF team)
- Disorders of tyrosine metabolism [ICD-10 Sub-category (who)]
- Tyrosinaemia type 1 [ICD-11 Sub-sub category]
Currated CISMeF NLP mapping
- Tyrosinosis [OMIM Phenotype]
- Tyrosinosis (disorder) [SNOMED CT concept]
- tyrosinosis [Disease (Nov.)]
- tyrosinosis, nos [SNOMED Notion]
- tyrosinosis, nos [TUV Concept]
MeSH term(s) associated for indexing
- amino acid metabolism, inborn errors [MeSH Descriptor]
Record concept(s)
- tyrosinosis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Tyrosinosis [OMIM Phenotype]
- Tyrosinosis (disorder) [SNOMED CT concept]
- tyrosinosis [Disease (Nov.)]
- tyrosinosis, nos [SNOMED Notion]
- tyrosinosis, nos [TUV Concept]
Validated automatic mappings to NTBT
- Disorders of tyrosine metabolism [ICD-10 Sub-category]

Keyword's position in hierarchy(ies) :

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04/05/2025

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