Term Name: neurodevelopmental disorder with involuntary movements
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.
Ontology: Human Disease [DOID:0112276]   ( DOID:0112276 )

Relationships
is a type of: autosomal dominant disease movement disease