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:
expandovarian disease (MONDO:0005558)
..Starting node
..expandovarian dysfunction ()

       Child Nodes:
........expandhyperestrogenism ()
........expandpremature menopause ()



 Sister 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 ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:1889
Name:ovarian dysfunction
Definition:The inability of the ovaries to function.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:ovarian failure; ovarian hypofunction; ovarian insufficiency
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal