Deafness, Autosomal Dominant 31 (DFNA31)

Alias:

Dfna31

Autosomal Dominant Nonsyndromic Deafness 31

Autosomal Dominant Deafness 31

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 31, also known as dfna31, is related to contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a and deafness, autosomal dominant 13. An important gene associated with Deafness, Autosomal Dominant 31 is DFNA31 (Deafness, Autosomal Dominant 31). Related phenotype is old-aged sensorineural hearing impairment.

Related ID：

MALACARDS：DFN154

OMIM：608645