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: fallopian tube carcinoma (MONDO:0006206)
..Starting node ..fallopian tube adenocarcinoma ()
Child Nodes:
........fallopian tube clear cell adenocarcinoma ()
........fallopian tube endometrioid adenocarcinoma ()
........fallopian tube mucinous adenocarcinoma ()
........fallopian tube papillary adenocarcinoma ()
........fallopian tube serous adenocarcinoma ()
Sister Nodes:
..fallopian tube adenocarcinoma ()
..fallopian tube carcinosarcoma ()
..fallopian tube gestational choriocarcinoma ()
..fallopian tube squamous cell carcinoma ()
..fallopian tube transitional cell carcinoma ()
..hereditary fallopian tube carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2746
Name:	fallopian tube adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the fallopian tube
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of fallopian tube; adenocarcinoma of the fallopian tube; fallopian tube adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal