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GTR Home > Conditions/Phenotypes > Intellectual disability, autosomal dominant 33

Intellectual disability, autosomal dominant 33

Synonyms
INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 33

Summary

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DPP6 gene. [from MONDO]

Available tests

8 tests are in the database for this condition.

Clinical tests (8 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: DPL1, DPPX, MRD33, VF2, DPP6
    Summary: dipeptidyl peptidase like 6

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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