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Cortical dysplasia, complex, with other brain malformations 13
rareAny autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DYNC1H1 gene.
- Identifiers
- MONDO:0013805 OMIM:614563
- Part of
- Autosomal dominant syndromic intellectual disabilityComplex cortical dysplasia with other brain malformationsDyneinopathy
- Also known as
- autosomal dominant non-syndromic intellectual disability caused by mutation in DYNC1H1 · DYNC1H1 autosomal dominant non-syndromic intellectual disability · DYNC1H1-NDD · DYNC1H1-related neurodevelopmental disorder · intellectual disability, autosomal dominant 13
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