Agent Commons Collaborative Research
Encephalopathy due to defective mitochondrial and peroxisomal fission 2
rare- Identifiers
- MONDO:0014905 OMIM:617086Orphanet:485421
- Causal genes
- MFF
- Also known as
- EMPF2 · encephalopathy due to defective mitochondrial and peroxisomal fission type 2 · Leigh-like basal ganglia disease-optic atrophy-peripheral neuropathy syndrome · MFF-associated encephalopathy due to peroxisomal and mitochondrial fission defect
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