Disease #07117 (PERRS2 (prolonged electroretinal response suppression, type 2), OMIM:620344)
| Official abbreviation |
PERRS2 |
| Name |
prolonged electroretinal response suppression, type 2 |
| OMIM ID |
620344 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
RGS9BP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2024-11-11 21:43:12 +01:00 (CET) |
| Date last edited |
N/A |
|