MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: adenocarcinoma (MONDO:0004970)
Parent Node: digestive system carcinoma (MONDO:0006181)
..Starting node ..gastroesophageal junction adenocarcinoma ()
Child Nodes:
Sister Nodes:
..ameloblastic carcinoma ()
..carcinoma of esophagus ()
..carcinoma of floor of mouth ()
..carcinoma of liver and intrahepatic biliary tract ()
..carcinoma of pharynx ()
..colorectal carcinoma ()
..digestive system mixed adenoneuroendocrine carcinoma ()
..exocrine pancreatic carcinoma ()
..gallbladder carcinoma ()
..gastric carcinoma ()
..gastroesophageal junction adenocarcinoma ()
..intestine carcinoma in situ ()
..maxillary sinus carcinoma ()
..oral cavity carcinoma ()
..pancreatic endocrine carcinoma ()
..small intestine carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3219
Name:	gastroesophageal junction adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the esophagogastric junction.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma - GEJ; adenocarcinoma of cardioesophageal junction; adenocarcinoma of gastroesophageal junction; adenocarcinoma of the cardioesophageal junction; adenocarcinoma of the EG junction; adenocarcinoma of the esophagogastric junction; adenocarcinoma of the gastroesophageal junction; adenoca
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal