keratoglobus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Limbus-to-limbus corneal thinning, often greatest in the periphery, with globular protrusion of the cornea. (Human Phenotype Ontology, HP_0001119)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001119
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Genes

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

Symbol Name
PIEZO2 piezo-type mechanosensitive ion channel component 2
PRDM5 PR domain containing 5
ZNF469 zinc finger protein 469