Deafness, Autosomal Recessive 12 (DFNB12)

Alias:

Deafness, Autosomal Recessive 12, Modifier of

Dfnb12

Autosomal Recessive Nonsyndromic Deafness 12

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 12

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 12

Congenital Neurosensory Deafness Autosomal Recessive 12

Autosomal Recessive Nonsyndromic Hearing Loss 12

Deafness, Autosomal Recessive, Type 12

Deafness, Autosomal Recessive, 12

Autosomal Recessive Deafness 12

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 12, also known as dfnb12, is related to usher syndrome, type if and nonsyndromic hearing loss. An important gene associated with Deafness, Autosomal Recessive 12 is CDH23 (Cadherin Related 23), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Affiliated tissues include brain, and related phenotypes are prelingual sensorineural hearing impairment and rod-cone dystrophy

Related ID：

MALACARDS：DFN141

OMIM：601386

MESH：D006319