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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

Disease Browser
Parent Node: Adnexal Diseases (D000291)
Parent Node: Gonadal Disorders (D006058)
..Starting node ..Ovarian Diseases (D010049)
Child Nodes:
........Anovulation (D000858)
........Chondrodysplasia, acromesomelic, with genital anomalies (C537913)
........Menopause, Premature (D008594) 1
........Oophoritis (D009869) 1
........Ovarian Cysts (D010048) 5
........OVARIAN DYSGENESIS 1 (OMIM:233300)
........Ovarian Hyperstimulation Syndrome (D016471)
........Ovarian Neoplasms (D010051) 25
........Primary Ovarian Insufficiency (D016649) 9
........Vanishing White Matter Leukodystrophy with Ovarian Failure (C565836)
Sister Nodes:
..Disorders of Sex Development (D012734) 107
..Female Athlete Triad Syndrome (D053716)
..Hypogonadism (D007006) 62
..Ovarian Diseases (D010049) 51
..Puberty, Delayed (D011628) 1
..Puberty, Precocious (D011629) 8
..Testicular Diseases (D013733) 28
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8483
Name:	Ovarian Diseases
Definition:	Pathological processes of the OVARY.
Alternative IDs:
ParentIDs:	MESH:D000291\|MESH:D006058
TreeNumbers:	C13.351.500.056.630 \|C19.391.630
Synonyms:	Disease, Ovarian \|Diseases, Ovarian \|Ovarian Disease
Slim Mappings:	Endocrine system disease\|Urogenital disease (female)
Reference:	MedGen: D010049 MeSH: D010049 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants