Disease #01715 (ACHM2 (achromatopsia, type 2 (ACHM-2)), OMIM:216900)
| Official abbreviation |
ACHM2 |
| Name |
achromatopsia, type 2 (ACHM-2) |
| OMIM ID |
216900 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
5 |
| Associated with 1 gene |
CNGA3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|