Term Name:	neurodevelopmental disorder with speech delay, movement abnormalities, and seizures
Synonyms:
Definition:	An autosomal dominant intellectual developmental disorder characterized by motor delay with mildly delayed walking, variably impaired intellectual development with poor or absent speech, behavioral abnormalities, early-onset seizures, and movement abnormalities, including tremor, ataxia, and dyskinesias that has_material_basis_in heterozygous mutation in the UNC13A gene on chromosome 19p13.
Ontology:	Human Disease [DOID:0061253]   ( DOID:0061253 )