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GTR Home > Conditions/Phenotypes > Autosomal recessive nonsyndromic hearing loss 29

Autosomal recessive nonsyndromic hearing loss 29

Synonyms
DFNB29 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal recessive 29

Summary

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CLDN14 gene. [from MONDO]

Available tests

22 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (22 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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