| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Lack of transparency of the corneal epithelium. (Human Phenotype Ontology, HP_0007727) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0007727 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the opacification of the corneal epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ALDH3A2 | aldehyde dehydrogenase 3 family, member A2 |
