FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term dystonia 25 ID (Ontology) DOID:0090055 (Human Disease)
Definition A multifocal dystonia that is characterized by cervical, laryngeal and hand-forearm dystonia, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the GNAL gene on chromosome 18p11.
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 Genes
 dystonia 25       2
 for disease ribbon | dystonia 25       2
 model of | dystonia 25       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
dystonia                        |
 |__multifocal dystonia_________|
                                dystonia 25  2 rec.
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Is a autosomal dominant disease
multifocal dystonia
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ICD10CM:G24.1
MIM:615073
ORDO:329466