neonatal severe cardiopulmonary failure due to mitochondrial methylation defect (Q55784996)
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human disease
- Combined Oxidative Phosphorylation Deficiency type 28
- Combined oxidative phosphorylation defect type 28
- COXPD28
- Combined Oxidative Phosphorylation Deficiency 28
- combined oxidative phosphorylation deficiency 28
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | neonatal severe cardiopulmonary failure due to mitochondrial methylation defect |
human disease |
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