Intellectual disability, autosomal dominant 33

MONDO:0014580

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DPP6 gene.

Also known as: DPP6 autosomal dominant non-syndromic intellectual disability, MRD33, autosomal dominant intellectual disability 33, autosomal dominant non-syndromic intellectual disability caused by mutation in DPP6, intellectual disability, autosomal dominant 33, intellectual disability, autosomal dominant type 33, mental retardation, autosomal dominant type 33, autosomal dominant non-syndromic intellectual disability 33

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal dominant 33 itself.

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Including sub-types (0) Tagged with Intellectual disability, autosomal dominant 33 (0)

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