Disease #00518
Official abbreviation |
616539 |
Name |
Combined oxidative phosphorylation deficiency 26, 616539 (3) |
OMIM ID |
616539 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
TRMT5 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|