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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: Pelvic Organ Prolapse (D056887)
Parent Node: Uterine Diseases (D014591)
..Starting node ..Uterine Prolapse (D014596)
Child Nodes:
Sister Nodes:
..Adenomyosis (D062788)
..Endometrial Hyperplasia (D004714)
..Endometritis (D004716)
..Hematometra (D006409)
..McKusick Kaufman syndrome (C538159)
..Progesterone Resistance (C564871)
..Pyometra (D055112)
..Uterine Cervical Diseases (D002577) 12
..Uterine Hemorrhage (D014592) 3
..Uterine Inversion (D019687)
..Uterine Neoplasms (D014594) 13
..Uterine Prolapse (D014596)
..Uterine Retroversion (D060725)
..Uterine Rupture (D014597) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11476
Name:	Uterine Prolapse
Definition:	Downward displacement of the UTERUS. It is classified in various degrees: in the first degree the UTERINE CERVIX is within the vaginal orifice; in the second degree the cervix is outside the orifice; in the third degree the entire uterus is outside the orifice.
Alternative IDs:
ParentIDs:	MESH:D014591\|MESH:D056887
TreeNumbers:	C13.351.500.852.833 \|C23.300.842.624.750
Synonyms:	Prolapses, Uterine \|Prolapses, Vaginal \|Prolapse, Uterine \|Prolapse, Vaginal \|Uterine Prolapses \|Vaginal Prolapse \|Vaginal Prolapses
Slim Mappings:	Pathology (anatomical condition)\|Urogenital disease (female)
Reference:	MedGen: D014596 MeSH: D014596 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants