Disease #00520
Official abbreviation |
616794 |
Name |
Combined oxidative phosphorylation deficiency 28, 616794 (3) |
OMIM ID |
616794 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
SLC25A26 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|