| 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) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0011520 |
| Similar Terms | |
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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 |
