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GTR Home > Conditions/Phenotypes > Odonto-onycho-dermal dysplasia

Odonto-onycho-dermal dysplasia

Synonyms
Odontoonychodermal dysplasia
Modes of inheritance
Autosomal recessive inheritance (Orphanet)

Summary

Odontoonychodermal dysplasia (OODD) is an autosomal recessive disorder characterized by dry hair, severe hypodontia, smooth tongue with marked reduction of fungiform and filiform papillae, onychodysplasia, hyperkeratosis of the palms and soles, hypo- and hyperhidrosis of the skin, and atrophic patches on the face (summary by Adaimy et al., 2007; Yu et al., 2019). [from OMIM]

Available tests

29 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (29 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ECTD16, OODD, SSPS, STHAG4, WNT10A
    Summary: Wnt family member 10A

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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