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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 Diseases (D010049)
Parent Node: Pelvic Inflammatory Disease (D000292)
..Starting node ..Oophoritis (D009869)
Child Nodes:
........Autoimmune oophoritis (C538274)
Sister Nodes:
..Endometritis (D004716)
..Fitz-Hugh-Curtis syndrome (C537936)
..Oophoritis (D009869) 1
..Parametritis (D010249)
..Salpingitis (D012488)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8246
Name:	Oophoritis
Definition:	Inflammation of the OVARY, generally caused by an ascending infection of organisms from the endocervix.
Alternative IDs:
ParentIDs:	MESH:D000292\|MESH:D010049
TreeNumbers:	C13.351.500.056.630.450 \|C13.351.500.056.750.500 \|C19.391.630.450
Synonyms:	Oophoritides
Slim Mappings:	Endocrine system disease\|Urogenital disease (female)
Reference:	MedGen: D009869 MeSH: D009869 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants