valinemia - CISMeF

Preferred Label : valinemia;

MeSH synonym : valine transaminase deficiency; hypervalinemia;

Origin ID

C536524;

UMLS CUI

C0268573;

Automatic exact mappings (from CISMeF team)
- Other disorders of branched-chain amino-acid metabolism [ICD-10 Sub-category]
- Other disorders of branched-chain amino-acid metabolism [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Hypervalinaemia [ICD-11 More detail]
- Hypervalinemia [HPO term]
- Hypervalinemia (disorder) [SNOMED CT concept]
- Valinemia [OMIM Phenotype]
- hypervalinemia [SNOMED Notion]
HPO term
- Hypervalinemia [HPO term]
MeSH term(s) associated for indexing
- amino acid metabolism, inborn errors [MeSH Descriptor]
- valine [MeSH Descriptor]
Record concept(s)
- Valinemia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypervalinaemia [ICD-11 More detail]
- Hypervalinemia [HPO term]
- Hypervalinemia (disorder) [SNOMED CT concept]
- Valinemia [OMIM Phenotype]
- hypervalinemia [SNOMED Notion]