Deafness, Autosomal Recessive 77 (DFNB77)

Alias:

Dfnb77

Autosomal Recessive Nonsyndromic Deafness 77

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 77

Autosomal Recessive Nonsyndromic Hearing Loss 77

Deafness, Autosomal Recessive, Type 77

Deafness, Autosomal Recessive, 77

Autosomal Recessive Deafness 77

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 77, also known as dfnb77, is related to non-syndromic genetic deafness and nonsyndromic hearing loss. An important gene associated with Deafness, Autosomal Recessive 77 is LOXHD1 (Lipoxygenase Homology PLAT Domains 1), and among its related pathways/superpathways is Sensory processing of sound. Related phenotypes are bilateral sensorineural hearing impairment and tinnitus

Related ID：

MALACARDS：DFN108

OMIM：613079

MESH：D003638