Deafness, Autosomal Dominant 30 (DFNA30)

Deafness, Autosomal Dominant 30(来自ICD-11)

别称:

Dfna30

Autosomal Dominant Nonsyndromic Deafness 30

Autosomal Dominant Deafness 30

加入收藏

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 30, also known as dfna30, is related to contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a and deafness, autosomal recessive 16. An important gene associated with Deafness, Autosomal Dominant 30 is DFNA30 (Deafness, Autosomal Dominant 30). Related phenotype is sensorineural hearing impairment.

查看原文参与反馈