Disease #00512
Official abbreviation |
614932 |
Name |
Combined oxidative phosphorylation deficiency 13, 614932 (3) |
OMIM ID |
614932 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
PNPT1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|