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Standards Ontologies Notations
polycystic ovary syndrome

Summary
Synonym
  • Multicystic ovaries
  • PCOS
  • Polycystic Ovarian disease
  • Polycystic ovaries
  • Stein-Leventhal synd.
  • Stein-Leventhal syndrome
  • polycystic ovary
Definition
An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight.
Super Class
ovarian dysfunction
External Links
Disease Ontology
DOID:11612
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 61 - 70 of 107 in total
Gene ID Gene Symbol Description Source
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5291 PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
5294 PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
5310 PKD1 polycystin 1, transient receptor potential channel interacting
5329 PLAUR plasminogen activator, urokinase receptor
5538 PPT1 palmitoyl-protein thioesterase 1
5563 PRKAA2 protein kinase AMP-activated catalytic subunit alpha 2
5728 PTEN phosphatase and tensin homolog
5743 PTGS2 prostaglandin-endoperoxide synthase 2
Displaying all 3 entries
Gene ID Gene Symbol Description Source
11450 Adipoq adiponectin, C1Q and collagen domain containing
11652 Akt2 thymoma viral proto-oncogene 2
12846 Comt catechol-O-methyltransferase
Displaying all 2 entries
Gene ID Gene Symbol Description Source
24267 Comt catechol-O-methyltransferase
25233 Akt2 AKT serine/threonine kinase 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
851974 YPR1 trifunctional aldehyde reductase/carbonyl reductase (NADPH)/glucose 1-dehydrogenase (NADP(+)) YPR1
Related Glycoprotein
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: August 19, 2024