" /> Deafness, autosomal dominant 25 - CISMeF





Preferred Label : Deafness, autosomal dominant 25;

Symbol : DFNA25;

CISMeF acronym : DFNA25;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the solute carrier family 17 (vesicular glutamate cotransporter), member 8 gene (SLC17A8, 607557.0001);

Prefixed ID : #605583;

Details


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03/05/2025


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