Deafness, Autosomal Recessive 106 (DFNB106)

Alias:

Deafness Autosomal Recessive 106

Dfnb106

Hearing Loss, Autosomal Recessive 106

Deafness, Autosomal Recessive, 106

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 106, is also known as deafness autosomal recessive 106. An important gene associated with Deafness, Autosomal Recessive 106 is EPS8L2 (EPS8 Signaling Adaptor L2). Affiliated tissues include brain, and related phenotype is hearing impairment.

Related ID：

MALACARDS：DFN361

OMIM：617637

MESH：D006319