peripheral opacification of the cornea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduced transparency of the peripheral region of the cornea. (Human Phenotype Ontology, HP_0008011)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008011
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Genes

7 genes associated with the peripheral opacification of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALDH18A1 aldehyde dehydrogenase 18 family, member A1
APOB apolipoprotein B
CHRDL1 chordin-like 1
EPHX2 epoxide hydrolase 2, cytoplasmic
KERA keratocan
LDLR low density lipoprotein receptor
MMP2 matrix metallopeptidase 2