Deafness, Autosomal Recessive 68 (DFNB68)

Alias:

Dfnb68

Autosomal Recessive Nonsyndromic Hearing Loss 68

Autosomal Recessive Nonsyndromic Deafness 68

Deafness, Autosomal Recessive, Type 68

Deafness, Autosomal Recessive, 68

Autosomal Recessive Deafness 68

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 68, also known as dfnb68, is related to deafness, autosomal recessive 35. An important gene associated with Deafness, Autosomal Recessive 68 is S1PR2 (Sphingosine-1-Phosphate Receptor 2). Affiliated tissues include brain, and related phenotype is sensorineural hearing impairment.

Related ID：

MALACARDS：DFN263

OMIM：610419

MESH：D006319