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GTR Home > Conditions/Phenotypes > Tietz syndrome

Tietz syndrome

Synonyms
Albinism-deafness of Tietz; Hypopigmentation/deafness of Tietz; Tietz albinism-deafness syndrome
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

Tietz albinism-deafness syndrome (TADS) is characterized by generalized pigment loss and congenital complete sensorineural hearing loss (summary by Izumi et al., 2008). [from OMIM]

Available tests

40 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (40 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CMM8, COMMAD, MI, MITF-A, WS2, WS2A, bHLHe32, MITF
    Summary: melanocyte inducing transcription factor

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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