Intellectual disability, autosomal dominant 3

MONDO:0012946

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CDH15 gene.

Also known as: CDH15 autosomal dominant non-syndromic intellectual disability, MRD3, autosomal dominant intellectual disability 3, autosomal dominant non-syndromic intellectual disability caused by mutation in CDH15, intellectual disability, autosomal dominant 3, intellectual disability, autosomal dominant type 3, mental retardation, autosomal dominant type 3, autosomal dominant non-syndromic intellectual disability 3

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal dominant 3 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 3 (0)

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