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The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.
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Hereditary Hearing Loss (DFNB1)
Hereditary Hearing Loss (DFNB1)
Prevalence:
~18M
otologic
Official
·
OMIM:220290
Official
·
ORPHA90635
The most common form of hereditary deafness caused by mutations in the GJB2 gene.
Associated Genes
GJB2
Gap Junction Protein Beta 2
Chromosome 13
Autosomal Recessive