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

Term ID:	7821
Name:	Neonatal ovarian cyst
Definition:
Alternative IDs:
ParentIDs:	MESH:D010048
TreeNumbers:	C04.182.612/C536396 \|C13.351.500.056.630.580/C536396 \|C19.391.630.580/C536396
Synonyms:	Fetal ovarian cyst
Slim Mappings:	Cancer\|Endocrine system disease\|Urogenital disease (female)
Reference:	MedGen: C536396 MeSH: C536396 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants