opacification of the corneal epithelium Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Lack of transparency of the corneal epithelium. (Human Phenotype Ontology, HP_0007727)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007727
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Genes

1 genes associated with the opacification of the corneal epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALDH3A2 aldehyde dehydrogenase 3 family, member A2