Disease #00117
Official abbreviation |
PEOA1 |
Name |
Progressive external ophthalmoplegia, autosomal dominant, 157640 (3) |
OMIM ID |
157640 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
POLG |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|