Disease #00090
Official abbreviation |
COQ10D1 |
Name |
Coenzyme Q10 deficiency, primary, 1, 607426 (3) |
OMIM ID |
607426 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
COQ2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|