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: ureter benign neoplasm (MONDO:0001398)
Parent Node: urothelial papilloma (MONDO:0004041)
..Starting node ..ureter urothelial papilloma ()
Child Nodes:
........ureter inverted papilloma ()
Sister Nodes:
..bladder urothelial papilloma ()
..inverted urothelial papilloma ()
..renal pelvis urothelial papilloma ()
..ureter urothelial papilloma ()
..urethral urothelial papilloma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4044
Name:	ureter urothelial papilloma
Definition:	A benign epithelial neoplasm that produces visible warty projections from the epithelial surface of the ureter.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	ureter urothelial papilloma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal