Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant
Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant
Definition
Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIN1 gene.
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, mental retardation, autosomal dominant 8, mental retardation, autosomal dominant 8, formerly, mental retardation, autosomal dominant type 8, MRD8, NDHMSD, neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant — per MONDO