macular retinal pigment epithelial mottling Gene Set

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
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Genes

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