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GTR Home > Conditions/Phenotypes > Intellectual disability, autosomal dominant 4

Intellectual disability, autosomal dominant 4

Summary

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the KIRREL3 gene. [from MONDO]

Available tests

9 tests are in the database for this condition.

Clinical tests (9 available)

Molecular Genetics Tests

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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