Fatal encephalopathy, lactic acidosis, and severe mitochondrial dna depletion in muscle

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Subtype of: Mitochondrial dna depletion syndrome
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • fatal encephalopathy, lactic acidosis, and severe mitochondrial DNA depletion in muscle
MONDO_0014198
FBXL4 Unknown
23993194
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Fatal encephalopathy, lactic acidosis, and severe mitochondrial dna depletion in muscle.
5 View disease cluster →
Mitochondrial encephalomyopathy 1 shared geneFBXL4 Related via 1 shared gene including FBXL4. Mitochondrial dna depletion syndrome 1 shared geneFBXL4 Related via 1 shared gene including FBXL4. Moyamoya angiopathy 1 shared geneFBXL4 Related via 1 shared gene including FBXL4. Leigh syndrome 1 shared geneFBXL4 Related via 1 shared gene including FBXL4. Mitochondrial disease 1 shared geneFBXL4 Related via 1 shared gene including FBXL4.