aminomethyltransferase

Preferred Label : aminomethyltransferase;

Approved symbol HGNC : AMT;

Name synonyms HGNC : glycine cleavage system protein T; nonketotic hyperglycinemia;

Alias symbols HGNC : NKH; GCST;

Chromosome HGNC : 3p21.31;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000145020;

Details

Origin ID

HGNC:473;

UMLS CUI

C1412390;

Automatic exact mappings (from CISMeF team)
- Aminomethyltransferase [OMIM gene]
- Aminomethyltransferase (substance) [SNOMED CT concept]
- Glycine Encephalopathy [NCIt concept]
- Glycine encephalopathy [ORDO Disease]
- Glycine encephalopathy 1 [OMIM Phenotype]
- Non-ketotic hyperglycinemia (disorder) [SNOMED CT concept]
- Nonketotic hyperglycinemia [MedDRA LLT]
- Nonketotic hyperglycinemia [HPO term]
- aminomethyltransferase [ORDO Gene]
- aminomethyltransferase [MeSH concept]
- aminomethyltransferase [SNOMED Notion]
- aminomethyltransferase [MeSH Descriptor]
- glycine encephalopathy [DO Concept]
- hyperglycinemia, nonketotic [MeSH concept]
- hyperglycinemia, nonketotic [MeSH Descriptor]
OMIM gene
- Aminomethyltransferase [OMIM gene]
Orphanet gene
- aminomethyltransferase [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Aminomethyltransferase [OMIM gene]

Keyword's position in hierarchy(ies) :

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