Intellectual disability, autosomal dominant 41

MONDO:0014842

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the TBL1XR1 gene.

Also known as: MRD41, TBL1XR1 autosomal dominant non-syndromic intellectual disability, autosomal dominant intellectual disability 41, autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1, intellectual disability, autosomal dominant 41, intellectual disability, autosomal dominant type 41, mental retardation, autosomal dominant 41, mental retardation, autosomal dominant type 41

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal dominant 41 itself.

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↑ Autosomal dominant non-syndromic intellectual disability (8)

Including sub-types (0) Tagged with Intellectual disability, autosomal dominant 41 (0)

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