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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: Ovarian Diseases (D010049)
..Starting node ..Anovulation (D000858)
Child Nodes:
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:	740
Name:	Anovulation
Definition:	Suspension or cessation of OVULATION in animals or humans with follicle-containing ovaries (OVARIAN FOLLICLE). Depending on the etiology, OVULATION may be induced with appropriate therapy.
Alternative IDs:
ParentIDs:	MESH:D010049
TreeNumbers:	C13.351.500.056.630.050 \|C19.391.630.050
Synonyms:	Anovulations
Slim Mappings:	Endocrine system disease\|Urogenital disease (female)
Reference:	MedGen: D000858 MeSH: D000858 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants