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: adenoma (MONDO:0004972)
Parent Node: glandular cell neoplasm (MONDO:0024276)
..Starting node ..villous adenoma ()
Child Nodes:
........duodenal villous adenoma ()
........rectal villous adenoma ()
........urethral villous adenoma ()
........urinary bladder villous adenoma ()
........vaginal villous adenoma ()
........villous adenoma of colon ()
Sister Nodes:
..adenocarcinoma ()
..cystadenoma ()
..glandular papilloma ()
..mucinous neoplasm ()
..oncocytic neoplasm () L: 00167;
..rete ovarii adenoma ()
..serous neoplasm ()
..vaginal glandular neoplasm ()
..villous adenoma ()
..vulvar glandular neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	502
Name:	villous adenoma
Definition:	An epithelial neoplasm morphologically characterized by the presence of a villous architectural pattern. Most often it occurs in the large intestine, small intestine, and the stomach in which the neoplastic epithelial cells show dysplastic features. It may also arise in the urinary bladder, urethra, and vagina.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	villous adenoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal