Deafness, Autosomal Recessive 21 (DFNB21)

Deafness, Autosomal Recessive 21(来自ICD-11)

别称:

Dfnb21

Autosomal Recessive Nonsyndromic Deafness 21

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 21

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 21

Autosomal Recessive Nonsyndromic Hearing Loss 21

Deafness, Autosomal Recessive, Type 21

Deafness, Autosomal Recessive, 21

Autosomal Recessive Deafness 21

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 21, also known as dfnb21, is related to deafness, autosomal recessive 42 and deafness, autosomal recessive 24. An important gene associated with Deafness, Autosomal Recessive 21 is TECTA (Tectorin Alpha), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and nervous system

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