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Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17: Disease Bioinformatics

Research of Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 has been linked to Dysplasia, Complete Hearing Loss, Deafness Congenital, Nerve Degeneration, Sensorineural Hearing Loss (disorder). The study of Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 has been mentioned in research publications which can be found using our bioinformatics tool below. Browse our catalog of research reagents for Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 including antibodies and ELISA kits.

Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 below! For more information on how to use Laverne, please read the How to Guide.
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Related Diseases

Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 has been studied in relation to diseases such as:

Alternate Names

Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 is also known as Late-onset Progressive Hereditary Hearing Impairment Due To Cochleosaccular Degeneration.