| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. (Human Disease Ontology, DOID_10584) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C538365 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Retinitis pigmentosa 1 from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| RP1 | retinitis pigmentosa 1 (autosomal dominant) | 2.88009 |
