decreased serum leptin Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A decreased concentration of leptin in the blood. (Human Phenotype Ontology, HP_0003292)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003292
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Genes

3 genes associated with the decreased serum leptin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
LEP leptin