Intellectual disability, autosomal dominant 39

MONDO:0014678

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the MYT1L gene.

Also known as: MRD39, MYT1L autosomal dominant non-syndromic intellectual disability, autosomal dominant intellectual disability 39, autosomal dominant non-syndromic intellectual disability caused by mutation in MYT1L, intellectual developmental disorder, autosomal dominant 39, intellectual disability, autosomal dominant 39, intellectual disability, autosomal dominant type 39, mental retardation, autosomal dominant type 39

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