| Label | Id | |
|---|---|---|
| achromatopsia 3; ACHM3 | http://purl.obolibrary.org/obo/MONDO_0009875 | |
| achromatopsia caused by mutation in CNGB3 | 9875 | |
| Beckwith-Wiedemann syndrome due to 11p15 microduplication | 19875 | |
| achromatopsia with myopia | 9875 | |
| total colorblindness with myopia | 9875 |