Deafness, Autosomal Recessive 101 (DFNB101)

Deafness, Autosomal Recessive 101(来自ICD-11)

别称:

Dfnb101

Autosomal Recessive Nonsyndromic Deafness 101

Autosomal Recessive Nonsyndromic Hearing Loss 101

Deafness, Autosomal Recessive, Type 101

Deafness, Autosomal Recessive, 101

Autosomal Recessive Deafness 101

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 101, also known as dfnb101, is related to autosomal recessive nonsyndromic deafness 36 and deafness, autosomal recessive 22. An important gene associated with Deafness, Autosomal Recessive 101 is GRXCR2 (Glutaredoxin And Cysteine Rich Domain Containing 2), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Related phenotypes are bilateral sensorineural hearing impairment and visual impairment

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