insulin - CISMeF

Preferred Label : insulin;

Approved symbol HGNC : INS;

Chromosome HGNC : 11p15.5;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000254647;

Details

Origin ID

HGNC:6081;

UMLS CUI

C1337112;

Automatic exact mappings (from CISMeF team)
- Insulin [OMIM gene]
- Insulin [FMA entity]
- Insulin [NCIt concept]
- Insulin [MedDRA LLT]
- Insulin [LOINC component]
- Insulin [ICNP mean]
- Insulin (substance) [SNOMED CT concept]
- Insulin Measurement [NCIt concept]
- Insulin Sensitivity Measurement [NCIt concept]
- Insulin regular [LOINC component]
- Therapeutic Insulin [NCIt concept]
- diabetes medicines [MedlinePlus Topic]
- insulin [ORDO Gene]
- insulin [SNOMED Notion]
- insulin [LOINC Challenge]
- insulin [MeSH Descriptor]
- insulin [Substance BNPC]
- insulin [MeSH concept]
- insulin [Artificial nutrition thesaurus concept]
- insulin [EMDN type]
- insulins [MeSH concept]
- insulins [MeSH Descriptor]
NCIt concept
- INS Gene [NCIt concept]
OMIM gene
- Insulin [OMIM gene]
Orphanet gene
- insulin [ORDO Gene]
See also inter- (CISMeF)
- Insulin [SMS substance]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- INS Gene [NCIt concept]
- INS gene [LOINC component]
- Insulin [OMIM Phenotype]
- Insulin [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

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