corneal perforation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A rupture of the cornea through which a portion of the iris protrudes. (Human Phenotype Ontology, HP_0100583)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100583
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3