primary coenzyme Q10 deficiency 2 (Q60195089)
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A primary coenzyme Q10 deficiency that has material basis in an autosomal recessive mutation of PDSS1 on chromosome 10p12.1.
- COQ10D2
- coenzyme Q10 deficiency, primary, 2
- hearing loss-encephaloneuropathy-obesity-valvulopathy syndrome
- deafness-encephaloneuropathy-obesity-valvulopathy syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | primary coenzyme Q10 deficiency 2 |
A primary coenzyme Q10 deficiency that has material basis in an autosomal recessive mutation of PDSS1 on chromosome 10p12.1. |
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