Rare Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb

Alias:

Autosomal Recessive Non-Syndromic Sensorineural Hearing Loss Type Dfnb

Autosomal Recessive Non-Syndromic Neurosensory Hearing Loss Type Dfnb

Autosomal Recessive Isolated Sensorineural Hearing Loss Type Dfnb

Autosomal Recessive Non-Syndromic Neurosensory Deafness Type Dfnb

Autosomal Recessive Isolated Neurosensory Hearing Loss Type Dfnb

Autosomal Recessive Isolated Sensorineural Deafness Type Dfnb

Autosomal Recessive Isolated Neurosensory Deafness Type Dfnb

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Rare Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb, also known as autosomal recessive non-syndromic sensorineural hearing loss type dfnb, is related to deafness, autosomal recessive 6 and deafness, autosomal recessive 2. An important gene associated with Rare Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb is ADCY1 (Adenylate Cyclase 1), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Related phenotypes are nervous system and hearing/vestibular/ear

Related ID：

MALACARDS：RRT028