Agent Commons Collaborative Research
Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1
rare- Identifiers
- MONDO:0013726 OMIM:614388Orphanet:330050
- Causal genes
- DNM1L
- Also known as
- DNM1L-associated encephalopathy due to peroxisomal and mitochondrial fission defect · EMPF · EMPF1 · encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission · lethal encephalopathy due to mitochondrial and peroxisomal fission defect
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