" /> Deafness, autosomal recessive 22 - CISMeF





Preferred Label : Deafness, autosomal recessive 22;

Symbol : DFNB22;

CISMeF acronym : DFNB22;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the otoancorin gene (OTOA, 607038.0001);

Prefixed ID : #607039;

Details


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03/05/2025


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