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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: Cysts (D003560)
Parent Node: Ovarian Diseases (D010049)
..Starting node ..Ovarian Cysts (D010048)
Child Nodes:
........Fraser-Like Syndrome (C565562)
........Neonatal ovarian cyst (C536396)
........Polycystic Ovary Syndrome (D011085) 2
Sister 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)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8482
Name:	Ovarian Cysts
Definition:	General term for CYSTS and cystic diseases of the OVARY.
Alternative IDs:
ParentIDs:	MESH:D003560\|MESH:D010049
TreeNumbers:	C04.182.612 \|C13.351.500.056.630.580 \|C19.391.630.580
Synonyms:	Corpus Luteum Cyst \|Corpus Luteum Cysts \|Cyst, Corpus Luteum \|Cyst, Ovarian \|Cysts, Corpus Luteum \|Cysts, Ovarian \|Ovarian Cyst
Slim Mappings:	Cancer\|Endocrine system disease\|Urogenital disease (female)
Reference:	MedGen: D010048 MeSH: D010048 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants