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: cystic neoplasm (MONDO:0021077)
Parent Node: glandular cell neoplasm (MONDO:0024276)
..Starting node ..cystadenoma ()
Child Nodes:
........bile duct cystadenoma ()
........mucinous cystadenoma ()
........ovarian cystadenoma ()
........pancreatic cystadenoma ()
........papillary cystadenoma ()
........seminal vesicle cystadenoma ()
........serous cystadenoma ()
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:	2369
Name:	cystadenoma
Definition:	A benign or borderline cystic epithelial neoplasm arising from the glandular epithelium. The epithelial cells line the cystic spaces which contain serous or mucinous fluid. Representative examples include ovarian and pancreatic cystadenomas.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	cystadenoma; cystadenoma (morphologic abnormality); cystadenoma, benign; cystoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal