|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of anomalous trichromacy associated with abnormal M photopigment, such that the absorption spectrum is shifted toward L wavelengths. Affected individuals have difficulties distinguishing between red and green. (Human Phenotype Ontology, HP_0011520)|
|Downloads & Tools|
1 genes associated with the deuteranomoly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|OPN1MW||opsin 1 (cone pigments), medium-wave-sensitive|