Leigh syndrome with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase

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Subtype of: Leigh syndrome
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Leigh syndrome with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase
MONDO_0014576
LIPT1 Unknown
24256811 24341803 27247813
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Leigh syndrome with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase.
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Lipoyltransferase deficiency 1 shared geneLIPT1 Related via 1 shared gene including LIPT1. Leigh syndrome 1 shared geneLIPT1 Related via 1 shared gene including LIPT1. Hearing loss 1 shared geneLIPT1 Related via 1 shared gene including LIPT1.