Deafness, Autosomal Dominant 44 (DFNA44)

Alias:

Dfna44

Autosomal Dominant Nonsyndromic Deafness 44

Autosomal Dominant Nonsyndromic Hearing Loss 44

Deafness, Autosomal Dominant, Type 44

Deafness, Autosomal Dominant, 44

Autosomal Dominant Deafness 44

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 44, also known as dfna44, is related to nonsyndromic hearing loss and sensorineural hearing loss. An important gene associated with Deafness, Autosomal Dominant 44 is CCDC50 (Coiled-Coil Domain Containing 50), and among its related pathways/superpathways is Sensory processing of sound. Related phenotypes are sensorineural hearing impairment and abnormality of the inner ear

Related ID：

MALACARDS：DFN118

OMIM：607453

MESH：D003638