Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CACNG2 gene.
Comprehensive, easy-to-understand information about this condition
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intellectual disability, autosomal dominant 1
MONDO:0007974
intellectual disability, autosomal dominant 3
MONDO:0012946
intellectual disability, autosomal dominant 4
MONDO:0012947
intellectual disability, autosomal dominant 5
MONDO:0012960
intellectual disability, autosomal dominant 6
MONDO:0013509
intellectual disability, autosomal dominant 2
MONDO:0013581