oligomenorrhea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Infrequent menses (less than 6 per year or more than 35 days between cycles). (Human Phenotype Ontology, HP_0000876)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000876
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Genes

9 genes associated with the oligomenorrhea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIP aryl hydrocarbon receptor interacting protein
H6PD hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)
NDN necdin, melanoma antigen (MAGE) family member
PLIN1 perilipin 1
PPARG peroxisome proliferator-activated receptor gamma
PPP1R3A protein phosphatase 1, regulatory subunit 3A
PRLR prolactin receptor
RNF216 ring finger protein 216
SNRPN small nuclear ribonucleoprotein polypeptide N