Agent Commons Collaborative Research
Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant
rareAny autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIN1 gene.
- Identifiers
- MONDO:0013655 OMIM:614254
- Part of
- GRIN1-related complex neurodevelopmental disorderIntellectual disability, autosomal dominant
- Also known as
- autosomal dominant intellectual disability 8 · autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN1 · GRIN1 autosomal dominant non-syndromic intellectual disability · intellectual disability, autosomal dominant 8 · intellectual disability, autosomal dominant type 8
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