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: ovarian disease (MONDO:0005558)
..Starting node ..ovarian cyst (disease) ()
Child Nodes:
........corpus luteum cyst ()
........malignant ovarian cyst ()
........neonatal ovarian cyst ()
Sister Nodes:
..anovulation ()
..luteoma of pregnancy ()
..oophoritis ()
..ovarian cyst (disease) ()
..ovarian dysfunction ()
..ovarian ectopic pregnancy ()
..ovarian endometriosis ()
..ovarian hyperstimulation syndrome ()
..ovarian neoplasm ()
..ovarian remnant syndrome ()
..ovarian stromal hyperthecosis ()
..primary ovarian failure ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3282
Name:	ovarian cyst (disease)
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	corpus luteum cyst; corpus luteum cysts; cyst, corpus luteum; cyst, ovarian; cysts, corpus luteum; cysts, ovarian; ovarian cyst
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal