Deafness, Autosomal Recessive 18a (DFNB18A)

Alias:

Deafness, Autosomal Recessive 18

Dfnb18a

Autosomal Recessive Nonsyndromic Deafness 18a

Dfnb18

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 18

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 18

Autosomal Recessive Nonsyndromic Hearing Loss 18a

Deafness, Autosomal Recessive, Type 18a

Deafness, Autosomal Recessive, 18a

Autosomal Recessive Deafness 18a

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 18a, also known as deafness, autosomal recessive 18, is related to usher syndrome, type ic and nonsyndromic hearing loss. An important gene associated with Deafness, Autosomal Recessive 18a is USH1C (USH1 Protein Network Component Harmonin), and among its related pathways/superpathways are Olfactory Signaling Pathway and Ciliary landscape. Affiliated tissues include brain and retina, and related phenotypes are nervous system and hearing/vestibular/ear

Related ID：

MALACARDS：DFN247

OMIM：602092

MESH：D006319