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Human Disease

neurodevelopmental disorder with involuntary movements

Term ID
DOID:0112276
Synonyms
  • NEDIM
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. (2)
References
Ontology
Human Disease   ( DOID:0112276 )
Relationships
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Genes Involved
Zebrafish Models