Autosomal Recessive Nonsyndromic Deafness 36

Alias:

Deafness, Autosomal Recessive 36, with or Without Vestibular Involvement

Deafness, Autosomal Recessive 36

Autosomal Recessive Deafness 36

Dfnb36

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Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Autosomal Recessive Nonsyndromic Deafness 36, also known as deafness, autosomal recessive 36, with or without vestibular involvement, is related to deafness, autosomal recessive 36, with or without vestibular involvement and usher syndrome, type iid. An important gene associated with Autosomal Recessive Nonsyndromic Deafness 36 is ESPN (Espin), and among its related pathways/superpathways are Olfactory Signaling Pathway and Ciliary landscape. Related phenotypes are nervous system and hearing/vestibular/ear

Related ID：

MALACARDS：ATS380