FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term dystonia 22, adult-onset ID (Ontology) DOID:0060967 (Human Disease)
Definition A dystonia characterized by focal dystonia or tremor and mild cognitive impairment that has_material_basis_in homozygous missense mutation in the TSPOAP1 gene.
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 Genes
 dystonia 22, adult-onset       1
 for disease ribbon | dystonia 22, adult-onset       1
 model of | dystonia 22, adult-onset       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
movement disease                 |
 |__dystonia_____________________|
                                 dystonia 22, adult-onset  1 rec.
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Is a autosomal recessive disease
dystonia
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MIM:620456