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: ureter carcinoma (MONDO:0006481)
..Starting node ..ureter adenocarcinoma ()
Child Nodes:
Sister Nodes:
..carcinoma in situ of ureter ()
..regional ureteric cancer ()
..ureter adenocarcinoma ()
..ureter small cell carcinoma ()
..ureter squamous cell carcinoma ()
..ureter transitional cell carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3216
Name:	ureter adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the ureter
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of the ureter; adenocarcinoma of ureter; ureter adenocarcinoma; ureteral adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal