central opacification of the cornea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduced transparency of the central portion of the corneal stroma. (Human Phenotype Ontology, HP_0011493)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011493
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4 genes associated with the central opacification of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL18A1 collagen, type XVIII, alpha 1
JAG1 jagged 1
NOD2 nucleotide-binding oligomerization domain containing 2
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4