FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term neurodevelopmental disorder with involuntary movements ID (Ontology) DOID:0112276 (Human Disease)
Definition A movement disease characterized by delayed psychomotor development and infantile or childhood onset of hyperkinetic involuntary movements, including chorea and athetosis that has_material_basis_in heterozygous mutation of the GNAO1 gene on chromosome 16q13.
Also Known As "NEDIM"
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 Genes
 neurodevelopmental disorder with involuntary movements       1
 for disease ribbon | neurodevelopmental disorder with involuntary movements       1
 model of | neurodevelopmental disorder with involuntary movements       1
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autosomal genetic disease
 |__autosomal dominant disease__
brain disease                   |
 |__movement disease____________|
                                neurodevelopmental disorder with involuntary movements  1 rec.
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Is a autosomal dominant disease
movement disease
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Synonyms
  • "NEDIM" EXACT OMO:0003012
Secondary IDs
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MIM:617493