Intellectual disability, autosomal dominant 10

MONDO:0013657

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CACNG2 gene.

Also known as: CACNG2 autosomal dominant non-syndromic intellectual disability, MRD10, autosomal dominant intellectual disability 10, autosomal dominant non-syndromic intellectual disability caused by mutation in CACNG2, intellectual disability, autosomal dominant 10, intellectual disability, autosomal dominant type 10, mental retardation, autosomal dominant type 10, autosomal dominant non-syndromic intellectual disability 10

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