Disease #00074
Official abbreviation |
PEOA3 |
Name |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 3; PEOA3 |
OMIM ID |
609286 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 2 genes |
C10orf2, TWNK |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|