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GTR Home > Conditions/Phenotypes > Autosomal recessive nonsyndromic hearing loss 103

Autosomal recessive nonsyndromic hearing loss 103

Synonyms
Deafness, autosomal recessive 103

Summary

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CLIC5 gene. [from MONDO]

Available tests

10 tests are in the database for this condition.

Clinical tests (10 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: DFNB102, DFNB103, MST130, MSTP130, CLIC5
    Summary: chloride intracellular channel 5

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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