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Entry Name Description Category Pathway Gene
H01365 Leber hereditary optic neuropathy and dystonia Leber hereditary optic neuropathy and dystonia (LDYT) is a maternally-inherited mitochondrial disorder characterized by variable combinations of visual loss and progressive generalized dystonia. LDYT is ... Inherited metabolic disorder MT-ND6 [HSA:4541] [KO:K03884]
MT-ND4 [HSA:4538] [KO:K03881]
MT-ND1 [HSA:4535] [KO:K03878]
MT-ND3 [HSA:4537] [KO:K03880]
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