Deafness, Autosomal Dominant 49 (DFNA49)

Alias:

Dfna49

Autosomal Dominant Nonsyndromic Deafness 49

Autosomal Dominant Deafness 49

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 49, also known as dfna49, is related to contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a and deafness, autosomal dominant 7. An important gene associated with Deafness, Autosomal Dominant 49 is DFNA49 (Deafness, Autosomal Dominant 49).

Related ID：

MALACARDS：DFN158

OMIM：608372