Deafness, Autosomal Recessive 116 (DFNB116)

Alias:

Dfnb116

Hearing Loss, Autosomal Recessive 116

Deafness, Autosomal Recessive, 116

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 116, also known as dfnb116, is related to autosomal recessive nonsyndromic deafness 116. An important gene associated with Deafness, Autosomal Recessive 116 is CLDN9 (Claudin 9). Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and global developmental delay

Related ID：

MALACARDS：DFN387

OMIM：619093

MESH：D006319