spermine synthase

Preferred Label : spermine synthase;

Approved symbol HGNC : SMS;

Alias symbols HGNC : MRSR; SPMSY; SpS;

Chromosome HGNC : Xp22.11;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000102172;

Details

Origin ID

HGNC:11123;

UMLS CUI

C1420262;

Automatic exact mappings (from CISMeF team)
- Smith-magenis syndrome [OMIM Phenotype]
- Spermine synthase [OMIM gene]
- Spermine synthase (substance) [SNOMED CT concept]
- spermine synthase [ORDO Gene]
- spermine synthase [MeSH Descriptor]
- spermine synthase [MeSH concept]
- spermine synthase [SNOMED Notion]
OMIM gene
- Spermine synthase [OMIM gene]
Orphanet gene
- spermine synthase [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Spermine synthase [OMIM gene]

Keyword's position in hierarchy(ies) :

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