1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0050957 | spinocerebellar ataxia type 4 | An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and peripheral neuropathy that has_material_basis_in heterozygous trinucleotide repeat expansion (GGCn) in the ZFHX3 gene on chromosome 16q22. |