| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Mottled (spotted or blotched with different shades) pigmentary abnormality of the macula lutea. (Human Phenotype Ontology, HP_0007793) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0007793 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the macular retinal pigment epithelial mottling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| PROM1 | prominin 1 |
