Disease

autosomal recessive nonsyndromic deafness 1B

Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12.
Synonyms
  • autosomal recessive deafness 1B
  • DFNB1B
Cross References
Parent Terms
Child Terms
None
Sources of Associations

Associated Genes

Associated Alleles

Associated Models