primary coenzyme Q10 deficiency 5 (Q60195093)
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primary coenzyme Q10 deficiency that has material basis in an autosomal recessive mutation of COQ9 on chromosome 16q21
- coenzyme Q10 deficiency, primary, 5
- COQ10D5
- ORDO:319678
- encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | primary coenzyme Q10 deficiency 5 |
primary coenzyme Q10 deficiency that has material basis in an autosomal recessive mutation of COQ9 on chromosome 16q21 |
|
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