|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A form of anterior segment dysgenesis in which abnormal cleavage of the anterior chamber occurs. Peters anomaly is characterized by central, paracentral, or complete corneal opacity. (Human Phenotype Ontology, HP_0000659)|
|Downloads & Tools|
3 genes associated with the peters anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.