Encephalopathy due to mitochondrial and peroxisomal fission defect

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
DNM1L-RELATED ENCEPHALOPATHY DUE TO MITOCHONDRIAL AND PEROXISOMAL FISSION DEFECT
330050
DNM1L Unknown
17460227
Orphanet, ClinGen
encephalopathy due to mitochondrial and peroxisomal fission defect
MFF Unknown — ClinGen —
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Encephalopathy due to mitochondrial and peroxisomal fission defect.
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Mitochondrial myopathy with sideroblastic anemia 1 shared geneDNM1L Related via 1 shared gene including DNM1L. Mitochondrial encephalomyopathy 2 shared genesDNM1L, MFF Related via 2 shared genes including DNM1L, MFF. Exostoses 1 shared geneMFF Related via 1 shared gene including MFF. Ventricular dysfunction 1 shared geneMFF Related via 1 shared gene including MFF. Leigh syndrome 2 shared genesDNM1L, MFF Related via 2 shared genes including DNM1L, MFF.