Disease

autosomal recessive nonsyndromic deafness 32

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.
Synonyms
  • autosomal recessive deafness 105
  • autosomal recessive deafness 32
Cross References
Parent Terms
Child Terms
None
Sources of Associations

Associated Genes

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Associated Models