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)
Parent Node: pregnancy disorder (MONDO:0024575)
..Starting node ..luteoma of pregnancy ()
Child Nodes:
Sister Nodes:
..acute fatty liver of pregnancy ()
..aromatase deficiency ()
..chorea gravidarum ()
..funisitis ()
..gestational diabetes ()
..gestational trophoblastic disease ()
..hypertension, pregnancy-induced ()
..impetigo herpetiformis ()
..intrahepatic cholestasis ()
..luteoma of pregnancy ()
..malignancy diagnosed during pregnancy ()
..pemphigoid gestationis ()
..peripartum cardiomyopathy ()
..placenta disease ()
..polyhydramnios (disease) ()
..pregnancy disorder with abortive outcome ()
..pruritic urticarial papules and plaques of pregnancy ()
..puerperal disorder ()
..supine hypotensive syndrome ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4387
Name:	luteoma of pregnancy
Definition:	A non-neoplastic and self-limited condition that occurs during pregnancy. It is characterized by proliferation of luteinized stromal cells that replace the normal ovarian stromal cells. It is usually manifested with bilateral multinodular ovarian masses. Treatment is not required.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	leuteoma of pregnancy; luteoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: SLC38A8;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal