Cyclin d2 - CISMeF

Preferred Label : Cyclin d2;

Symbol : CCND2;

CISMeF acronym : CCND2;

Type : Gene;

Ensembl ID : ENSG00000118971;

Prefixed ID : *123833;

Details

Origin ID

123833;

UMLS CUI

C1413173;

Automatic exact mappings (from CISMeF team)
- CCND2 Gene [NCIt concept]
- G1/S-Specific Cyclin-D2 [NCIt concept]
- cyclin D2 [ORDO Gene]
- cyclin D2 [MeSH concept]
- cyclin D2 [MeSH Descriptor]
- cyclin D2 [HGNC gene]
HGNC gene
- cyclin D2 [HGNC gene]
NCIt concept(s)
- CCND2 Gene [NCIt concept]
- CCND2 wt Allele [NCIt concept]
- G1/S-Specific Cyclin-D2 [NCIt concept]
ORDO concept(s)
- cyclin D2 [ORDO Gene]
Phenotypes related
- Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CCND2 Gene [NCIt concept]
- cyclin D2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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