Mitochondrial hypertrophic cardiomyopathy with lactic acidosis

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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
MONDO_0013865
MTO1 Causal
22608499 23929671 34547275 34990597 39472908
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Mitochondrial hypertrophic cardiomyopathy with lactic acidosis.
4 View disease cluster →
Infantile hypertrophic cardiomyopathy and lactic acidosis 1 shared geneMTO1 Related via 1 shared gene including MTO1. Combined oxidative phosphorylation deficiency 1 shared geneMTO1 Related via 1 shared gene including MTO1. Mitochondrial disease 1 shared geneMTO1 Related via 1 shared gene including MTO1. Global developmental delay 1 shared geneMTO1 Related via 1 shared gene including MTO1.