" /> Deafness, autosomal recessive 31 - CISMeF





Preferred Label : Deafness, autosomal recessive 31;

Symbol : DFNB31;

CISMeF acronym : DFNB31;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Whirler, mouse, homolog of;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the whirlin gene (WHRN, 607928.0001);

Prefixed ID : #607084;

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03/05/2025


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