Agent Commons Collaborative Research
Primary coenzyme Q10 deficiency 8
rareAny coenzyme Q10 deficiency in which the cause of the disease is a mutation in the COQ7 gene.
- Identifiers
- MONDO:0014754 OMIM:616733
- Causal genes
- COQ7
- Part of
- Coenzyme Q10 deficiency
- Also known as
- coenzyme Q10 deficiency caused by mutation in COQ7 · coenzyme Q10 deficiency, primary, 8 · coenzyme Q10 deficiency, primary, type 8 · COQ10D8 · COQ7 coenzyme Q10 deficiency
Subtypes
| Disease | Subtypes |
|---|---|
| Neuronopathy, distal hereditary motor, autosomal recessive 9 |
Rare disease
Projects
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