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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] |
[ KEGG | DISEASE | DRUG | MEDICUS ] |