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: ectopic pregnancy (MONDO:0000755)
Parent Node: ovarian disease (MONDO:0005558)
..Starting node ..ovarian ectopic pregnancy ()
Child Nodes:
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:	44098
Name:	ovarian ectopic pregnancy
Definition:	An abnormal pregnancy in which the conception is implanted on the ovary.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	ectopic pregnancy of ovary; ovarian Pregnancies; ovarian pregnancy; ovary ectopic pregnancy; Pregnancies, ovarian
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal