Spermine synthase

Preferred Label : Spermine synthase;

Symbol : SMS;

CISMeF acronym : SMS;

Type : Gene;

Ensembl ID : ENSG00000102172;

Prefixed ID : *300105;

Details

Origin ID

300105;

UMLS CUI

C1420262;

Automatic exact mappings (from CISMeF team)
- RAI1 wt Allele [NCIt concept]
- Skolt Sami Language [NCIt concept]
- Spermine synthase (substance) [SNOMED CT concept]
- Stiff person spectrum disorder [ORDO Disease]
- retinoic acid induced 1 [ORDO Gene]
- retinoic acid induced 1 [HGNC gene]
- spermine synthase [ORDO Gene]
- spermine synthase [MeSH Descriptor]
- spermine synthase [MeSH concept]
- spermine synthase [SNOMED Notion]
- spermine synthase [HGNC gene]
- symbol withdrawn SMCR [HGNC gene]
- text messaging [MeSH Descriptor]
HGNC gene
- spermine synthase [HGNC gene]
ORDO concept(s)
- spermine synthase [ORDO Gene]
Phenotypes related
- Intellectual developmental disorder, X-linked, syndromic, snyder-robinson type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- spermine synthase [HGNC gene]

Keyword's position in hierarchy(ies) :

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