Deafness, Autosomal Recessive 111 (DFNB111)

Alias:

Dfnb111

Autosomal Recessive Nonsyndromic Deafness 111

Hearing Loss, Autosomal Recessive 111

Deafness, Autosomal Recessive, 111

Autosomal Recessive Deafness 111

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Medical Symptom

Gene & Mutation

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Disease Model

References Literature

Deafness, Autosomal Recessive 111, also known as dfnb111, is related to deafness, autosomal recessive and deafness, autosomal recessive 77. An important gene associated with Deafness, Autosomal Recessive 111 is MPZL2 (Myelin Protein Zero Like 2). Affiliated tissues include brain, and related phenotypes are progressive sensorineural hearing impairment and hearing/vestibular/ear

Related ID：

MALACARDS：DFN369

OMIM：618145

MESH：D006319