Metadata | |
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ID | DOID:0050969 |
Name | spinocerebellar ataxia type 18 |
Definition | An autosomal dominant cerebellar ataxia that is characterized by cerebellar ataxia and sensory neuropathy, has_material_basis_in mutation on chromosome 7q22-q23. https://rarediseases.info.nih.gov/diseases/9976/spinocerebellar-ataxia-18 |
Xrefs | |
Subsets |
DO_rare_slim |
Parent Relationships |