Autosomal Dominant Deafness 39 with Dentinogenesis Imperfecta 1
Autosomal Dominant Deafness 4
autosomal dominant nonsyndromic deafness 1
autosomal dominant nonsyndromic deafness 10
autosomal dominant nonsyndromic deafness 11
autosomal dominant nonsyndromic deafness 12
autosomal dominant nonsyndromic deafness 13
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has_material_basis_in mutation in the COL11A2 gene on chromosome 6p21. (DO)