Deafness, Autosomal Recessive 49 (DFNB49)

Alias:

Dfnb49

Autosomal Recessive Nonsyndromic Deafness 49

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 49

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 49

Autosomal Recessive Nonsyndromic Hearing Loss 49

Deafness, Autosomal Recessive, Type 49

Deafness, Autosomal Recessive, 49

Autosomal Recessive Deafness 49

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 49, also known as dfnb49, is related to sensorineural hearing loss and deafness, autosomal dominant 58. An important gene associated with Deafness, Autosomal Recessive 49 is MARVELD2 (MARVEL Domain Containing 2), and among its related pathways/superpathways are Sertoli-Sertoli Cell Junction Dynamics and Sensory processing of sound. Affiliated tissues include brain, and related phenotypes are prelingual sensorineural hearing impairment and nervous system

Related ID：

MALACARDS：DFN092

OMIM：610153

MESH：D006319