| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0011517 |
| Similar Terms | |
| 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.
