Disease #02016 (ACHM-3 (achromatopsia, type 3 (ACHM-3)), OMIM:262300)
| Official abbreviation |
ACHM-3 |
| Name |
achromatopsia, type 3 (ACHM-3) |
| OMIM ID |
262300 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CNGB3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|