Deafness, Autosomal Recessive 26 (DFNB26)

Alias:

Dfnb26

Autosomal Recessive Nonsyndromic Hearing Loss 26

Autosomal Recessive Nonsyndromic Deafness 26

Deafness, Autosomal Recessive, 26

Autosomal Recessive Deafness 26

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 26, also known as dfnb26, is related to deafness, autosomal recessive 26, modifier of and deafness, autosomal recessive 2. An important gene associated with Deafness, Autosomal Recessive 26 is GAB1 (GRB2 Associated Binding Protein 1). Affiliated tissues include brain, and related phenotype is sensorineural hearing impairment.

Related ID：

MALACARDS：DFN168

OMIM：605428

MESH：D006319