Deafness, mitochondrial, modifier of

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Subtype of: Deafness
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Deafness, mitochondrial, modifier of
MONDO_0010799
TRMU Unknown
27604308
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Deafness, mitochondrial, modifier of.
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Infantile liver failure 1 shared geneTRMU Related via 1 shared gene including TRMU. Deafness, aminoglycoside-induced 1 shared geneTRMU Related via 1 shared gene including TRMU. Liver failure 1 shared geneTRMU Related via 1 shared gene including TRMU. Leigh syndrome 1 shared geneTRMU Related via 1 shared gene including TRMU. Mitochondrial disease 1 shared geneTRMU Related via 1 shared gene including TRMU.