" /> Deafness, autosomal recessive 115 - CISMeF





Preferred Label : Deafness, autosomal recessive 115;

Symbol : DFNB115;

CISMeF acronym : DFNB115;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the sphingolipid transporter-2 gene (SPNS2, 612584.0001);

Prefixed ID : #618457;

Details


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28/03/2024


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