Stearoyl-coa desaturase

Preferred Label : Stearoyl-coa desaturase;

Symbol : SCD;

CISMeF acronym : SCD;

Type : Gene;

Alternative titles and symbols : SCD1; DELTA-9-DESATURASE; Fatty acid desaturase 5; FADS5;

Ensembl ID : ENSG00000099194;

Prefixed ID : *604031;

Details

Origin ID

604031;

UMLS CUI

C1419846;

Automatic exact mappings (from CISMeF team)
- Acyl-CoA Desaturase [NCIt concept]
- Doctor of Science [NCIt concept]
- SCD Gene [NCIt concept]
- SCD wt Allele [NCIt concept]
- Schnyder corneal dystrophy [ORDO Disease]
- Sickle cell disease without crisis [ICD-11 Subcategory]
- Stearoyl-CoA desaturase [MeSH concept]
- Sudden Cardiac Death [NCIt concept]
- fatty acid desaturase 3 [HGNC gene]
- solute carrier family 22 member 5 [ORDO Gene]
- solute carrier family 22 member 5 [HGNC gene]
- stearoyl-CoA desaturase [HGNC gene]
- stearoyl-coa desaturase [MeSH Descriptor]
HGNC gene
- stearoyl-CoA desaturase [HGNC gene]
NCIt concept(s)
- Acyl-CoA Desaturase [NCIt concept]
- SCD Gene [NCIt concept]
- SCD wt Allele [NCIt concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SCD Gene [NCIt concept]
- stearoyl-CoA desaturase [HGNC gene]

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