| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://www.omim.org/entry/604229 |
| Similar Terms | |
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3 genes associated with the peters anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.
