Please sign in to follow a disease.

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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal dominant non-syndromic intellectual disability (8)

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

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.