Disease #00049
Official abbreviation |
PEOA5 |
Name |
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 5, PEOA5 |
OMIM ID |
613077 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
RRM2B |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|