| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A fundus dystrophy that is characterized by discrete uniform white dots over the entire fundus with greatest density in the midperiphery and no macular involvement. (Human Disease Ontology, DOID_11105) |
| External Link | http://www.omim.org/entry/136880 |
| Similar Terms | |
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3 genes associated with the retinitis punctata albescens phenotype from the curated OMIM Gene-Disease Associations dataset.
