recurrent corneal erosions Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of recurrent corneal epithelial erosions. Although most corneal epithelial defects heal quickly, some may show recurrent ulcerations. (Human Phenotype Ontology, HP_0000495)
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12 genes associated with the recurrent corneal erosions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHST6 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6
CTNS cystinosin, lysosomal cystine transporter
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FOXC2 forkhead box C2
GJB2 gap junction protein, beta 2, 26kDa
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
MBTPS2 membrane-bound transcription factor peptidase, site 2
MPV17 MpV17 mitochondrial inner membrane protein
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
TGFBI transforming growth factor, beta-induced, 68kDa