Disease #00532
Official abbreviation |
617675 |
Name |
Myopathy, mitochondrial, and ataxia, 617675 (3) |
OMIM ID |
617675 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
MSTO1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|