Disease #04344 (OPA-8 (atrophy, optic?, type 8 (OPA-8)), OMIM:616289)
| Official abbreviation |
OPA-8 |
| Name |
atrophy, optic?, type 8 (OPA-8) |
| OMIM ID |
616289 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ACO2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
N/A |
|