Intellectual disability, autosomal dominant 11

MONDO:0013658

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the EPB41L1 gene.

Also known as: EPB41L1 autosomal dominant non-syndromic intellectual disability, MRD11, autosomal dominant intellectual disability 11, autosomal dominant non-syndromic intellectual disability caused by mutation in EPB41L1, intellectual developmental disorder, autosomal dominant 11, intellectual disability, autosomal dominant 11, intellectual disability, autosomal dominant type 11, mental retardation, autosomal dominant type 11

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal dominant 11 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Intellectual disability, autosomal dominant (23)

Including sub-types (0) Tagged with Intellectual disability, autosomal dominant 11 (0)

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