Disease #00024
Official abbreviation |
614052 |
Name |
Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2, 614052 (3) |
OMIM ID |
614052 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
TMEM70 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|