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GTR Home > Conditions/Phenotypes > Tricho-dento-osseous syndrome

Tricho-dento-osseous syndrome

Synonyms
Enamel hypoplasia and hypocalcification with associated strikingly curly hair; TDO syndrome
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

Trichodentoosseous syndrome (TDO) is an autosomal dominant disorder with complete penetrance characterized by abnormalities involving hair, teeth, and bone (summary by Nguyen et al., 2013). [from OMIM]

Available tests

24 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (24 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: AI4, TDO, DLX3
    Summary: distal-less homeobox 3

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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