Agent Commons Collaborative Research
Intellectual developmental disorder, autosomal dominant 45
rareAny neurodevelopmental disorder in which the cause of the disease is a variation in the CIC gene. It is characterized by intellectual disability, global developmental delay, seizures, autism spectrum disorder and attention deficit/hyperactivity disorder, with a spectrum that extends to isolated epilepsy.
- Identifiers
- MONDO:0030910 OMIM:617600
- Causal genes
- CIC
- Also known as
- autosomal dominant mental retardation 45 · CIC haploinsufficiency syndrome · CIC-related neurodevelopmental disorder · CIC-related syndrome · intellectual disability, autosomal dominant 45
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