| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A type of anomalous trichromacy associated with defective long-wavelength-sensitive (L) cones, causing the sensitivity spectrum to be shifted toward medium wavelengths. This leads to difficulties especially in distinguishing red and green. (Human Phenotype Ontology, HP_0200018) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0200018 |
| Similar Terms | |
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1 genes associated with the protanomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| OPN1LW | opsin 1 (cone pigments), long-wave-sensitive |
