Nucleolin - CISMeF

Preferred Label : Nucleolin;

Symbol : NCL;

CISMeF acronym : NCL;

Type : Gene;

Alternative titles and symbols : C23;

Ensembl ID : ENSG00000115053;

Prefixed ID : *164035;

Details

Origin ID

164035;

UMLS CUI

C1417613;

Automatic exact mappings (from CISMeF team)
- NCL Gene [NCIt concept]
- NCL wt Allele [NCIt concept]
- Neuronal ceroid lipofuscinosis [ORDO Disease]
- Neuronal ceroid lipofuscinosis [ICD-11 Subcategory]
- Nucleolin [NCIt concept]
- neuronal ceroid-lipofuscinoses [MeSH Descriptor]
- nucleolin [HGNC gene]
- nucleolin [MeSH concept]
False automatic mappings
- New Caledonia [NCIt concept]
HGNC gene
- nucleolin [HGNC gene]
NCIt concept(s)
- NCL Gene [NCIt concept]
- NCL wt Allele [NCIt concept]
- Nucleolin [NCIt concept]
See also inter- (CISMeF)
- Nucleolin [MeSH Descriptor]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NCL Gene [NCIt concept]
- nucleolin [HGNC gene]

Keyword's position in hierarchy(ies) :

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