Disease #00048
Official abbreviation |
610131 |
Name |
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4, 610131 (3) |
OMIM ID |
610131 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
POLG2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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