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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: Obstetric Labor Complications (D007744)
Parent Node: Uterine Diseases (D014591)
..Starting node ..Uterine Inversion (D019687)
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:	11473
Name:	Uterine Inversion
Definition:	A complication of OBSTETRIC LABOR in which the corpus of the UTERUS is forced completely or partially through the UTERINE CERVIX. This can occur during the late stages of labor and is associated with IMMEDIATE POSTPARTUM HEMORRHAGE.
Alternative IDs:
ParentIDs:	MESH:D007744\|MESH:D014591
TreeNumbers:	C13.351.500.852.726 \|C13.703.420.814
Synonyms:	Inversion of Uterus \|Inversion, Uterine \|Uterus Inversion
Slim Mappings:	Pregnancy complication\|Urogenital disease (female)
Reference:	MedGen: D019687 MeSH: D019687 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants