aminomethyltransferase

Preferred Label : aminomethyltransferase;

Origin ID

F-683A8;

UMLS CUI

C0103013;

Automatic exact mappings (from CISMeF team)
- Aminomethyltransferase [OMIM gene]
- aminomethyltransferase [MeSH Descriptor]
- aminomethyltransferase [MeSH concept]
- aminomethyltransferase [HGNC gene]
- aminomethyltransferase [ORDO Gene]
Currated CISMeF NLP mapping
- Aminomethyltransferase (substance) [SNOMED CT concept]
Décrit
- aminomethyltransferase deficiency [SNOMED Notion]
SNOMED CT concept
- Aminomethyltransferase (substance) [SNOMED CT concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]
UMLS correspondences (same concept)
- Aminomethyltransferase (substance) [SNOMED CT concept]
- aminomethyltransferase [MeSH Descriptor]
- aminomethyltransferase [MeSH concept]