Intellectual disability, autosomal dominant 5

MONDO:0012960

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the SYNGAP1 gene.

Also known as: MRD5, SYNGAP1 autosomal dominant non-syndromic intellectual disability, SYNGAP1-related developmental and epileptic encephalopathy, autosomal dominant intellectual disability 5, autosomal dominant non-syndromic intellectual disability caused by mutation in SYNGAP1, epilepsy due to SYNGAP mutations, intellectual disability, autosomal dominant 5, intellectual disability, autosomal dominant type 5

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