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GTR Home > Conditions/Phenotypes > Intellectual disability, autosomal dominant 3

Summary

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

Available tests

10 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: CDH14, CDH3, CDHM, MCAD, MRD3, CDH15
    Summary: cadherin 15

Clinical features

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