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: gallbladder carcinoma (MONDO:0003220)
..Starting node ..gallbladder adenocarcinoma ()
Child Nodes:
........gallbladder mucinous adenocarcinoma ()
........gallbladder papillary neoplasm with an associated invasive carcinoma ()
........gallbladder pleomorphic giant cell adenocarcinoma ()
........gallbladder signet ring cell adenocarcinoma ()
Sister Nodes:
..gall bladder carcinoma in situ ()
..gallbladder adenocarcinoma ()
..gallbladder small cell neuroendocrine carcinoma ()
..gallbladder squamous cell carcinoma ()
..undifferentiated gallbladder carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	6215
Name:	gallbladder adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the gall bladder.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of gallbladder; adenocarcinoma of the gallbladder; gall bladder adenocarcinoma; gallbladder adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal