Human genes for X-linked deafness 6
X-linked deafness 6 [DOID:0111740]
An X-linked nonsyndromic deafness characterized by severe bilateral sensorineural hearing loss with cochlear malformation in males and mild to moderate hearing loss in females with later onset that has_material_basis_in mutation in COL4A6 on chromosome Xq22.3.
Synonyms: X-linked deafness 6, DOID:0111740, Xlinked deafness 6, DFNX6