Severe x-linked mitochondrial encephalomyopathy

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Subtype of: Mitochondrial encephalomyopathy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
severe X-linked mitochondrial encephalomyopathy
MONDO_0010437
AIFM1 Causal
22019070 34117073 28967629 39472908
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Severe x-linked mitochondrial encephalomyopathy.
5 View disease cluster →
X-linked hereditary sensory and autonomic neuropathy with deafness 1 shared geneAIFM1 Related via 1 shared gene including AIFM1. Cowchock syndrome 1 shared geneAIFM1 Related via 1 shared gene including AIFM1. X-linked spondyloepimetaphyseal dysplasia 1 shared geneAIFM1 Related via 1 shared gene including AIFM1. Beta-hydroxyisobutyryl-coa deacylase deficiency 1 shared geneAIFM1 Related via 1 shared gene including AIFM1. Charcot-marie-tooth disease, x-linked 1 shared geneAIFM1 Related via 1 shared gene including AIFM1.