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: Uterine Diseases (D014591)
..Starting node ..Uterine Cervical Diseases (D002577)
Child Nodes:
........Uterine Cervical Dysplasia (D002578) 2
........Uterine Cervical Erosion (D002579)
........Uterine Cervical Incompetence (D002581)
........Uterine Cervical Neoplasms (D002583) 5
........Uterine Cervicitis (D002575)
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:	11464
Name:	Uterine Cervical Diseases
Definition:	Pathological processes of the UTERINE CERVIX.
Alternative IDs:
ParentIDs:	MESH:D014591
TreeNumbers:	C13.351.500.852.593
Synonyms:	Cervical Diseases, Uterine \|Cervical Disease, Uterine \|Cervix Disease \|Cervix Diseases \|Disease, Cervix \|Diseases, Cervix \|Diseases, Uterine Cervical \|Disease, Uterine Cervical \|Uterine Cervical Disease
Slim Mappings:	Urogenital disease (female)
Reference:	MedGen: D002577 MeSH: D002577 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants