encephalopathy due to defective mitochondrial and peroxisomal fission 2

Rare Disease

MONDO:0014905

Also known as:

EMPF2Leigh-like basal ganglia disease-optic atrophy-peripheral neuropathy syndromeMFF-associated encephalopathy due to peroxisomal and mitochondrial fission defect

Genes

Clinical Trials

1 active

Newborn Screening

–

Patient Groups

–

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Companies Active in encephalopathy due to defective mitochondrial and peroxisomal fission 2

0 approved

Organizations with approved therapies for this disease

No approved therapies yet

Research is ongoing — 1 company has orphan drug designations for this disease

Biostage, Inc.

Other

Designated

View all companies active in encephalopathy due to defective mitochondrial and peroxisomal fission 2

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encephalopathy due to defective mitochondrial and peroxisomal fission 2

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Companies Active in encephalopathy due to defective mitochondrial and peroxisomal fission 2

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