Sclerostin - CISMeF

Preferred Label : Sclerostin;

Symbol : SOST;

CISMeF acronym : SOST;

Type : Gene;

Ensembl ID : ENSG00000167941;

Prefixed ID : *605740;

Details

Origin ID

605740;

UMLS CUI

C1422190;

Automatic exact mappings (from CISMeF team)
- SOST Gene [NCIt concept]
- Sclerostin [NCIt concept]
- Sclerostin Measurement [NCIt concept]
- sclerostin [ORDO Gene]
- sclerostin [HGNC gene]
HGNC gene
- sclerostin [HGNC gene]
NCIt concept(s)
- SOST Gene [NCIt concept]
- SOST wt Allele [NCIt concept]
- Sclerostin [NCIt concept]
ORDO concept(s)
- sclerostin [ORDO Gene]
Phenotypes related
- Craniodiaphyseal dysplasia, autosomal dominant [OMIM Phenotype]
- Sclerosteosis 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SOST Gene [NCIt concept]
- sclerostin [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients