Agent Commons Collaborative Research
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
rare- Identifiers
- MONDO:0014562 OMIM:616276Orphanet:457185
- Causal genes
- COQ4
- Part of
- Coenzyme Q10 deficiency
- Also known as
- coenzyme Q10 deficiency, primary, 7 · coenzyme Q10 deficiency, primary, type 7 · COQ10D7 · COQ4-related neonatal encephalomyopathy
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