Table 1.

Summary of NuRD and CHD genes associated with neurodevelopmental disorders.

Gene	Neurodevelopmental Disorders
NuRD Subunits
CHD3	Craniofacial defects, developmental delay, language deficits (Snijders Blok–Campeau syndrome) [50]
CHD4	Developmental delay, speech and motor delay, cognitive impairment (Sifrim–Hitz–Weiss syndrome) [51,52]
CHD5	Language deficits, intellectual disability, epilepsy, behavioural disorder (Parenti–Mignot neurodevelopmental syndrome) [53]
GATAD2B	Motor disability, intellectual disability, language deficits, developmental delay, craniofacial abnormalities (GATAD2B-associated neurodevelopmental disorder) [54]
MBD3	Non-verbal ASD [55,56]
Other CHDs
CHD2	Epilepsy, neurobehavioural disorders, intellectual disability [57,58]
CHD7	Intellectual disability, hearing and visual impairments, developmental delay, self-injurious behaviour, sleep problems (CHARGE syndrome) [59,60,61]
CHD8	Developmental delay, ASD, behavioural disorder, musculoskeletal defects (Intellectual developmental disorder with autism and macrocephaly, IDDAM) [62,63,64]