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GTR Home > Conditions/Phenotypes > Autosomal recessive nonsyndromic hearing loss 39

Summary

An autosomal recessive disorder caused by mutations in the HGF gene, encoding hepatocyte growth factor. It is characterized by profound deafness. [from NCI]

Available tests

21 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: DFNB39, F-TCF, HGFB, HPTA, SF, HGF
    Summary: hepatocyte growth factor

Clinical features

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