Deafness, Autosomal Recessive 29 (DFNB29)

Alias:

Dfnb29

Autosomal Recessive Nonsyndromic Deafness 29

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 29

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 29

Autosomal Recessive Nonsyndromic Hearing Loss 29

Deafness, Autosomal Recessive, Type 29

Deafness, Autosomal Recessive, 29

Autosomal Recessive Deafness 29

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 29, also known as dfnb29, is related to deafness, autosomal recessive 24 and deafness, autosomal recessive 21. An important gene associated with Deafness, Autosomal Recessive 29 is CLDN14 (Claudin 14), and among its related pathways/superpathways are Integrin Pathway and Sertoli-Sertoli Cell Junction Dynamics. Affiliated tissues include brain, and related phenotypes are hearing impairment and sensorineural hearing impairment

Related ID：

MALACARDS：DFN139

OMIM：614035

MESH：D006319