Desmoglein 2 - CISMeF

Preferred Label : Desmoglein 2;

Symbol : DSG2;

CISMeF acronym : DSG2;

Type : Gene;

Alternative titles and symbols : Human desmoglein colon; HDGC;

Ensembl ID : ENSG00000046604;

Prefixed ID : *125671;

Details

Origin ID

125671;

UMLS CUI

C1414169;

Automatic exact mappings (from CISMeF team)
- DSG2 Gene [NCIt concept]
- DSG2 wt Allele [NCIt concept]
- Desmoglein-2 [NCIt concept]
- Hereditary diffuse gastric cancer [ORDO Disease]
- desmoglein 2 [ORDO Gene]
- desmoglein 2 [HGNC gene]
- desmoglein 2 [MeSH concept]
- desmoglein 2 [MeSH Descriptor]
HGNC gene
- desmoglein 2 [HGNC gene]
NCIt concept(s)
- DSG2 Gene [NCIt concept]
- DSG2 wt Allele [NCIt concept]
- Desmoglein-2 [NCIt concept]
ORDO concept(s)
- desmoglein 2 [ORDO Gene]
Phenotypes related
- Arrhythmogenic right ventricular dysplasia, familial, 10 [OMIM Phenotype]
- Cardiomyopathy, dilated, 1bb [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DSG2 Gene [NCIt concept]
- desmoglein 2 [HGNC gene]

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