Version: 8.0.0
Date: Tue Jan 28 2025
1 results
Disease Disease Group: monogenic disease Genes: CDC14 (Sce)

autosomal recessive nonsyndromic deafness 32

Disease
Source: DOID:0110491
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and male infertility in some affected men that has_material_basis_in mutation in the CDC14A gene on chromosome 1p21.2.
Genes: CDC14 (Sce)