Deafness, Autosomal Recessive 86 (DFNB86)

Alias:

Dfnb86

Autosomal Recessive Nonsyndromic Deafness 86

Deafness, Nonsyndromic, Autosomal Recessive, Type 86

Autosomal Recessive Nonsyndromic Hearing Loss 86

Deafness, Autosomal Recessive, 86

Autosomal Recessive Deafness 86

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 86, also known as dfnb86, is related to developmental and epileptic encephalopathy 16 and deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome. An important gene associated with Deafness, Autosomal Recessive 86 is TBC1D24 (TBC1 Domain Family Member 24), and among its related pathways/superpathways are Olfactory Signaling Pathway and Ciliary landscape. Related phenotypes are hearing impairment and nervous system

Related ID：

MALACARDS：DFN259

OMIM：614617

MESH：D006319