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GTR Home > Conditions/Phenotypes > Autosomal recessive nonsyndromic hearing loss 97

Summary

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

Genes See tests for all associated and related genes

  • Also known as: AUTS9, DA11, DFNB97, HGFR, RCCP2, c-Met, MET
    Summary: MET proto-oncogene, receptor tyrosine kinase

Clinical features

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