iris atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Atrophy of the iris. (Human Phenotype Ontology, HP_0001089)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001089
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Genes

2 genes associated with the iris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASPH aspartate beta-hydroxylase
LRP5 low density lipoprotein receptor-related protein 5