| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/180100 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the retinitis pigmentosa 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| RP1 | retinitis pigmentosa 1 (autosomal dominant) |
