Human genes for X-linked deafness 3
X-linked deafness 3 [DOID:0111736]
An X-linked nonsyndromic deafness characterized by congenital, bilateral, profound and sensorineural hearing loss in males and bilateral, mild to moderate high frequency sensorineural hearing impairment with later onset in heterozygous females that has_material_basis_in mutation in a region on chromosome Xp21.2.
Synonyms: X-linked deafness 3, DOID:0111736, Xlinked deafness 3, congenital sensorineural X-linked deafness 4, DFN4 ...