deuteranomoly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
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1 genes associated with the deuteranomoly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
OPN1MW opsin 1 (cone pigments), medium-wave-sensitive