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GTR Home > Conditions/Phenotypes > Intellectual disability, autosomal dominant 10

Intellectual disability, autosomal dominant 10

Summary

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CACNG2 gene. [from MONDO]

Available tests

6 tests are in the database for this condition.

Clinical tests (6 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: MRD10, CACNG2
    Summary: calcium voltage-gated channel auxiliary subunit gamma 2

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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