" /> Deafness, autosomal dominant 10 - CISMeF





Preferred Label : Deafness, autosomal dominant 10;

Symbol : DFNA10;

CISMeF acronym : DFNA10;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the EYA transcriptional coactivator and phosphatase 4 gene (EYA4, 603550.0001);

Prefixed ID : #601316;

Details


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03/05/2025


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