Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIN1 gene.

Also known as: GRIN1 autosomal dominant non-syndromic intellectual disability, MRD8, NDHMSD, autosomal dominant intellectual disability 8, autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN1, intellectual disability, autosomal dominant 8, intellectual disability, autosomal dominant type 8, mental retardation, autosomal dominant 8

1 clinical trial for this condition and its sub-types, 0 tagged with Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant itself.