Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 6
rareAny autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIN2B gene.
- Identifiers
- MONDO:0013509 OMIM:613970Orphanet:589547
- Part of
- GRIN2B-related complex neurodevelopmental disorderIntellectual disability, autosomal dominant
- Also known as
- autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN2B · GRIN2B autosomal dominant non-syndromic intellectual disability · GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder · intellectual developmental disorder, autosomal dominant 6, with or without seizures · intellectual disability, autosomal dominant type 6
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