Deafness, Autosomal Recessive 112 (DFNB112)

Alias:

Dfnb112

Autosomal Recessive Nonsyndromic Deafness 112

Hearing Loss, Autosomal Recessive 112

Deafness, Autosomal Recessive, 112

Autosomal Recessive Deafness 112

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 112, is also known as dfnb112. An important gene associated with Deafness, Autosomal Recessive 112 is BDP1 (B Double Prime 1, Subunit Of RNA Polymerase III Transcription Initiation Factor IIIB). Affiliated tissues include brain, and related phenotype is sensorineural hearing impairment.

Related ID：

MALACARDS：DFN371

OMIM：618257

MESH：D006319