MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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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: gastric carcinoma (MONDO:0004950)
..Starting node ..gastric adenocarcinoma ()
Child Nodes:
........diffuse gastric adenocarcinoma ()
........gastric cardia adenocarcinoma ()
........gastric intestinal type adenocarcinoma ()
........gastric papillary adenocarcinoma ()
........gastric tubular adenocarcinoma ()
........microinvasive gastric cancer ()
........mucinous gastric adenocarcinoma ()
........signet ring cell gastric adenocarcinoma ()
Sister Nodes:
..carcinoma of stomach, salivary gland type ()
..Epstein-Barr virus-associated gastric carcinoma ()
..gastric adenocarcinoma ()
..gastric body carcinoma ()
..gastric cardia carcinoma ()
..gastric fundus carcinoma ()
..gastric pylorus carcinoma ()
..gastric small cell neuroendocrine carcinoma ()
..gastric squamous cell carcinoma ()
..hereditary gastric cancer ()
..stomach carcinoma in situ ()
..undifferentiated carcinoma of stomach ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5036
Name:	gastric adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the stomach
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma - stomach; adenocarcinoma of stomach; adenocarcinoma of the stomach; gastric (stomach) adenocarcinoma; gastric adenocarcinoma; STAD; stomach adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal