Disease browser and phenotype portal

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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: Genital Diseases, Female (D005831)
..Starting node ..Uterine Diseases (D014591)
Child 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
Sister Nodes:
..Adnexal Diseases (D000291) 61
..Endometriosis (D004715)
..Gynatresia (D006175)
..Herpes Genitalis (D006558)
..Infertility (D007246) 26
..Reproductive Tract Infections (D060737)
..Sexual Dysfunction, Physiological (D012735) 5
..Sexually Transmitted Diseases (D012749) 41
..Tuberculosis, Female Genital (D014384)
..Uterine Diseases (D014591) 37
..Vaginal Diseases (D014623) 18
..Vulvar Diseases (D014845) 10
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11470
Name:	Uterine Diseases
Definition:	Pathological processes involving any part of the UTERUS.
Alternative IDs:
ParentIDs:	MESH:D005831
TreeNumbers:	C13.351.500.852
Synonyms:	Disease, Endometrial \|Diseases, Endometrial \|Diseases, Uterine \|Disease, Uterine \|Endometrial Disease \|Endometrial Diseases \|Uterine Disease
Slim Mappings:	Urogenital disease (female)
Reference:	MedGen: D014591 MeSH: D014591 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants