| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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://ctdbase.org/detail.go?type=disease&acc=MESH:C562733 |
| Similar Terms | |
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4 genes/proteins associated with the disease Fundus Albipunctatus from the curated CTD Gene-Disease Associations dataset.
