FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term spastic ataxia 1 ID (Ontology) DOID:0050772 (Human Disease)
Definition A spastic ataxia characterized by early-onset cerebellar ataxia, spasticity, pyramidal syndrome and peripheral neuropathy, has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the VAMP1 gene on chromosome 12p13.
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 spastic ataxia 1       1
 for disease ribbon | spastic ataxia 1       1
 model of | spastic ataxia 1       1
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autosomal genetic disease
 |__autosomal dominant disease__
hereditary ataxia               |
 |__spastic ataxia______________|
                                spastic ataxia 1  1 rec.
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Is a autosomal dominant disease
spastic ataxia
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MIM:108600