Intellectual disability, autosomal dominant 38

MONDO:0014617

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the EEF1A2 gene.

Also known as: EEF1A2 autosomal dominant non-syndromic intellectual disability, MRD38, PRELDS, autosomal dominant intellectual disability 38, autosomal dominant non-syndromic intellectual disability caused by mutation in EEF1A2, intellectual disability, autosomal dominant 38, intellectual disability, autosomal dominant type 38, mental retardation, autosomal dominant type 38

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