primary coenzyme Q10 deficiency 7 (Q60195095)
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A primary coenzyme Q10 deficiency that has material basis in an autosomal recessive mutation of COQ4 on chromosome 9q34.11.
- COQ10D7
- coenzyme Q10 deficiency, primary, 7
- COQ4-related neonatal encephalomyopathy
- neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | primary coenzyme Q10 deficiency 7 |
A primary coenzyme Q10 deficiency that has material basis in an autosomal recessive mutation of COQ4 on chromosome 9q34.11. |
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