Intellectual disability, autosomal dominant 6

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIN2B gene.

Also known as: GRIN2B encephalopathy, GRIN2B-related neurodevelopmental disorder, GRIN2B autosomal dominant non-syndromic intellectual disability, GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder, MRD6, autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN2B, intellectual developmental disorder, autosomal dominant 6, with or without seizures, intellectual disability, autosomal dominant 6

1 clinical trial for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal dominant 6 itself.