Search Ontology:
Human Disease
neurodevelopmental disorder with involuntary movements
- Term ID
- DOID:0112276
- Synonyms
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- 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 )
- is a type of
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Genes Involved
Zebrafish Models