Intellectual disability, autosomal dominant 3

rare

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

Identifiers: MONDO:0012946 OMIM:612580
Causal genes: CDH15
Part of: Intellectual disability, autosomal dominant
Also known as: autosomal dominant intellectual disability 3 · autosomal dominant non-syndromic intellectual disability caused by mutation in CDH15 · CDH15 autosomal dominant non-syndromic intellectual disability · intellectual disability, autosomal dominant type 3 · mental retardation, autosomal dominant 3

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