/autosomal recessive nonsyndromic hearing loss 32

autosomal recessive nonsyndromic hearing loss 32

Rare Disease

MONDO:0012091

Also Known As

CDC14A autosomal recessive nonsyndromic deafnessDFNB105DFNB32autosomal recessive deafness 105autosomal recessive deafness 32autosomal recessive nonsyndromic deafness 105autosomal recessive nonsyndromic deafness 32autosomal recessive nonsyndromic deafness caused by mutation in CDC14Aautosomal recessive nonsyndromic deafness type 105autosomal recessive nonsyndromic deafness type 32deafness, autosomal recessive 105deafness, autosomal recessive 32deafness, autosomal recessive 32, with or without immotile spermdeafness, autosomal recessive type 105

Definition

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in variation in the chromosome region 1p22.1-p13.3.