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: exocrine pancreatic carcinoma (MONDO:0005192)
..Starting node ..pancreatic adenocarcinoma ()
Child Nodes:
........pancreatic acinar cell carcinoma ()
........pancreatic cystadenocarcinoma ()
........pancreatic ductal adenocarcinoma ()
........pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma ()
........pancreatic tubular adenocarcinoma ()
Sister Nodes:
..familial pancreatic carcinoma ()
..osteoclastic giant cell tumor of pancreas ()
..pancreatic adenocarcinoma ()
..pancreatic carcinoma with mixed differentiation ()
..pancreatic intraductal papillary-mucinous carcinoma ()
..pancreatic large cell neuroendocrine carcinoma ()
..pancreatic mucinous cystadenoma ()
..solid pseudopapillary carcinoma of pancreas ()
..squamous cell carcinoma of pancreas ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	6047
Name:	pancreatic adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the pancreas
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma - pancreas; adenocarcinoma of pancreas; adenocarcinoma of the pancreas; PAAD; pancreas adenocarcinoma; pancreatic adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal