xanthelasma Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of xanthomata in the skin of the eyelid. (Human Phenotype Ontology, HP_0001114)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001114
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Genes

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

Symbol Name
APOB apolipoprotein B
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
EPHX2 epoxide hydrolase 2, cytoplasmic
LDLR low density lipoprotein receptor
LPL lipoprotein lipase
TTPA tocopherol (alpha) transfer protein