FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term dystonia 32 ID (Ontology) DOID:0060939 (Human Disease)
Definition A dystonia characterized by onset of symptoms in adulthood, sustained or intermittent muscle contractions causing abnormal movements or posturing. The disorder is slowly progressive with eventual generalized involvement of the limbs, trunk, neck, and larynx, resulting in dysarthria and dysphagia. Brain imaging may show abnormalities in the basal ganglia that has_material_basis_in homozygous mutation in the VPS11 gene on chromosome 11q23.
Also Known As "DYT32"
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 Genes
 dystonia 32       1
 for disease ribbon | dystonia 32       1
 model of | dystonia 32       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
movement disease                 |
 |__dystonia_____________________|
                                 dystonia 32  1 rec.
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Is a autosomal recessive disease
dystonia
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Synonyms
  • "DYT32" EXACT OMO:0003012
Secondary IDs
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MIM:619637