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: ovarian carcinoma (MONDO:0005140)
..Starting node ..ovarian adenocarcinoma ()
Child Nodes:
........Krukenberg carcinoma ()
........ovarian clear cell adenocarcinoma ()
........ovarian cystadenocarcinoma ()
........ovarian endometrioid adenocarcinoma ()
........ovarian mucinous adenocarcinoma ()
........ovarian serous adenocarcinoma ()
........rete ovarii adenocarcinoma ()
Sister Nodes:
..familial ovarian carcinoma ()
..ovarian adenocarcinoma ()
..ovarian carcinosarcoma ()
..ovarian large-cell neuroendocrine carcinoma ()
..ovarian small cell carcinoma ()
..ovarian squamous cell carcinoma ()
..ovarian transitional cell carcinoma ()
..ovary mixed epithelial carcinoma ()
..undifferentiated ovarian carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2752
Name:	ovarian adenocarcinoma
Definition:	An adenocarcinoma that arises from the ovary. It is the most common type of ovarian carcinoma. It includes the serous adenocarcinoma, mucinous adenocarcinoma, clear cell adenocarcinoma, and endometrioid adenocarcinoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of ovary; adenocarcinoma of the ovary; ovarian adenoacanthoma; ovarian adenocarcinoma; ovary adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal