Developmental delay with variable intellectual impairment and behavioral abnormalities
MONDO:0032745A neurodevelopmental disorder caused by a mutation in TCF gene, characterized by impaired intellectual development with speech difficulties and behavioral abnormalities, most commonly autism spectrum disorder (ASD), defects in attention, and/or hyperactivity.
Also known as: DDVIBA, TCF20-related disorder, TCF20-related syndrome, developmental delay with variable intellectual impairment and behavioral abnormalities
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