" /> Deafness, autosomal recessive 110 - CISMeF





Preferred Label : Deafness, autosomal recessive 110;

Symbol : DFNB110;

CISMeF acronym : DFNB110;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the cochlin gene (COCH, 603196.0010);

Prefixed ID : #618094;

Details


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04/05/2025


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