" /> Deafness, autosomal dominant 3b - CISMeF





Preferred Label : Deafness, autosomal dominant 3b;

Symbol : DFNA3B;

CISMeF acronym : DFNA3B;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the gap junction protein, beta-6 gene (GJB6, 604418.0001);

Prefixed ID : #612643;

Details


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03/05/2025


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