Leber Hereditary Optic Neuropathy And Dystonia
Disease ID: disease_node_20243
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| Dbxref | MIM:500001 |
|---|---|
| Subclassof | DOID_0111754 |
| Data Source | DOID |
| Synonyms | LDYT, Leber optic atrophy and dystonia, Leber optic atrophy with dystonia, Marsden syndrome, familial dystonia with visual failure and striatal lucencies |
| Doid Label | Leber hereditary optic neuropathy and dystonia |
| Doid Description | A Leber plus disease characterized by Leber hereditary optic neuropathy and dystonia that has_material_basis_in mutation in the mitochondrial genes MTND6, MTND4, MTND1 or MTND3 that make up the mitochondrial complex I. |
| Disease Node Id | disease_node_20243 |
| Doid Id | DOID_0111755 |
| Label | Leber Hereditary Optic Neuropathy And Dystonia |
- Outgoing r'ship
SUBCLASS_OFto/from Leber Plus Disease(ID:disease_node_20241) (Disease)