(Q50349610)
English
autosomal dominant non-syndromic intellectual disability 6
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GRIN2B on chromosome 12p13.1.
- MRD6
- autosomal dominant mental retardation 6
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 6
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 6; MRD6
- Mental Retardation, Autosomal Dominant type 6
- GRIN2B-related neurodevelopmental disorder
Statements
1 reference
Identifiers
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(2 entries)
- enwiki GRIN2B-related neurodevelopmental disorder
- fiwiki GRIN2B-oireyhtymä