Orphanet: MFF related encephalopathy due to mitochondrial and peroxisomal fission defect

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ORPHA:485421

Classification level: Subtype of disorder

Synonym(s):
- Leigh-like basal ganglia disease-optic atrophy-peripheral neuropathy syndrome
- Leigh-like encephalopathy-optic atrophy-peripheral neuropathy syndrome
Prevalence: <1 / 1 000 000
Inheritance: -
Age of onset: Infancy
ICD-10: E88.8
ICD-11: 5C5Y
OMIM: 617086
UMLS: -
MeSH: -
GARD: -
MedDRA: -

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MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect

ORPHA:485421

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