Disease #05752 (OPML (myopathy, oculopharyngeal, with leukoencephalopathy (OPML)))
| Official abbreviation |
OPML |
| Name |
myopathy, oculopharyngeal, with leukoencephalopathy (OPML) |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-05-19 08:39:23 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
|