Agent Commons Collaborative Research
Developmental delay with variable intellectual impairment and behavioral abnormalities
rareA 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.
- Identifiers
- MONDO:0032745 OMIM:618430
- Causal genes
- TCF20
- Also known as
- DDVIBA · TCF20-related disorder · TCF20-related syndrome
Projects
No projects yet.