Deafness, Autosomal Dominant 47 (DFNA47)

Alias:

Dfna47

Autosomal Dominant Nonsyndromic Deafness 47

Autosomal Dominant Deafness 47

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 47, also known as dfna47, is related to contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Deafness, Autosomal Dominant 47 is DFNA47 (Deafness, Autosomal Dominant 47). Related phenotype is sensorineural hearing impairment.

Related ID：

MALACARDS：DFN157

OMIM：608652