intellectual disability, autosomal dominant 3

Rare Disease

MONDO:0012946

Also known as:

CDH15 autosomal dominant non-syndromic intellectual disabilityMRD3autosomal dominant intellectual disability 3

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

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intellectual disability, autosomal dominant 3

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