MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandfemale reproductive system disease (MONDO:0002263)
Parent Node:
expandgonadal disease (MONDO:0002259)
..Starting node
..expandovarian disease ()

       Child Nodes:
........expandanovulation ()
........expandluteoma of pregnancy ()
........expandoophoritis ()
........expandovarian cyst (disease) ()
........expandovarian dysfunction ()
........expandovarian ectopic pregnancy ()
........expandovarian endometriosis ()
........expandovarian hyperstimulation syndrome ()
........expandovarian neoplasm ()
........expandovarian remnant syndrome ()
........expandovarian stromal hyperthecosis ()
........expandprimary ovarian failure ()



 Sister Nodes: 
..expandgonadoblastoma ()
..expandhypogonadism ()
..expandovarian disease ()
..expandprecocious puberty ()
..expandsex differentiation disease ()
..expandtesticular disease ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:5558
Name:ovarian disease
Definition:A disease involving the ovary.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:disease of ovary; disease or disorder of ovary; disorder of ovary; disorder of ovary; ovarian disease; ovarian disorder; ovary disease; ovary disease or disorder
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal