Aminomethyltransferase

Preferred Label : Aminomethyltransferase;

Symbol : AMT;

CISMeF acronym : AMT;

Type : Gene;

Alternative titles and symbols : Glycine cleavage system t protein; GCST;

Ensembl ID : ENSG00000145020;

Prefixed ID : *238310;

Détails

Origin ID

238310;

UMLS CUI

C1412390;

Automatic exact mappings (from CISMeF team)
- Abbreviated Mental Test Score (assessment scale) [SNOMED CT concept]
- Aminomethyltransferase (substance) [SNOMED CT concept]
- aminomethyltransferase [ORDO Gene]
- aminomethyltransferase [MeSH concept]
- aminomethyltransferase [HGNC gene]
- aminomethyltransferase [SNOMED Notion]
- aminomethyltransferase [MeSH Descriptor]
- blood pressure monitoring, ambulatory [MeSH Descriptor]
HGNC gene
- aminomethyltransferase [HGNC gene]
NCIt concept(s)
- AMT Gene [NCIt concept]
- AMT wt Allele [NCIt concept]
- Aminomethyltransferase, Mitochondrial [NCIt concept]
ORDO concept(s)
- aminomethyltransferase [ORDO Gene]
Phenotypes related
- Glycine encephalopathy 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- aminomethyltransferase [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients