Disease #00141
Official abbreviation |
MTATP6 |
Name |
ATP SYNTHASE 6;;MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1, INCLUDED |
OMIM ID |
516060 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 2 genes |
, MT-ATP6 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|