|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||The condition of having both rods and cones, but only a single kind of cone. Affected individuals have good pattern vision in daylight, but cannot distinguish between colors. (Human Phenotype Ontology, HP_0011517)|
|Downloads & Tools|
2 genes associated with the cone monochromacy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.