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GTR Home > Conditions/Phenotypes > Ectodermal dysplasia 13, hair/tooth type

Ectodermal dysplasia 13, hair/tooth type

Summary

Some ectodermal dysplasias are here classified as congenital disorders characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings. Ectodermal dysplasia-13 of the hair/tooth type is characterized by severe oligodontia accompanied by anomalies of hair and skin (Issa et al., 2016). [from OMIM]

Available tests

4 tests are in the database for this condition.

Clinical tests (4 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ECTD13, KREMEN, KRM1, KREMEN1
    Summary: kringle containing transmembrane protein 1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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