premature arteriosclerosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Arteriosclerosis occuring at an age that is younger than usual. (Human Phenotype Ontology, HP_0005177)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005177
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Genes

1 genes associated with the premature arteriosclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
WRN Werner syndrome, RecQ helicase-like