| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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://ctdbase.org/detail.go?type=disease&acc=MESH:C537884 |
| Similar Terms | |
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3 genes/proteins associated with the disease Peters anomaly from the curated CTD Gene-Disease Associations dataset.
