| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A congenital malformation of the anterior segment characterized by iridicorneal malformation, glaucoma, iris stroma hypoplasia, posterior embryotoxon, and corneal opacities. (Human Phenotype Ontology, HP_0000558) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0000558 |
| Similar Terms | |
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2 genes associated with the rieger anomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
