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: cystic neoplasm (MONDO:0021077)
..Starting node ..cystadenocarcinoma ()
Child Nodes:
........biliary cystadenocarcinoma ()
........mucinous cystadenocarcinoma ()
........ovarian cystadenocarcinoma ()
........pancreatic cystadenocarcinoma ()
........papillary cystadenocarcinoma ()
........serous cystadenocarcinoma ()
Sister Nodes:
..cystadenocarcinoma ()
..cystadenoma ()
..papillary cystic neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5596
Name:	cystadenocarcinoma
Definition:	A malignant cystic epithelial neoplasm arising from the glandular epithelium. The malignant epithelial cells invade the stroma. The cystic spaces contain serous or mucinous fluid. Representative examples include ovarian and pancreatic cystadenocarcinomas.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	cystadenocarcinoma; cystadenocarcinoma (morphologic abnormality); cystadenocarcinoma NOS (morphologic abnormality); cystadenocarcinoma, malignant
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal