AB51ICD-11 MMS 2026-01
Acquired hearing impairment
Description
Loss of hearing that occurs sometime the course of life and is not present at birth. The hearing impairment is sustained after the acquisition of language, which can occur due to disease, trauma, or as a side-effect of a medicine. Conductive hearing loss may occur as a result of a problem in the outer or middle ear such as an obstruction (cerumen, foreign body), damage to the ossicles, middle ear infections, and/or perforation of the tympanic membrane. Sensorineural hearing loss is a type of hearing loss in which the root cause lies in the vestibulocochlear nerve (Cranial nerve VIII), the inner ear, or central processing centres of the brain. Mixed conductive and sensorineural hearing loss refers to a mix of both conductive and sensorineural hearing loss.
Excludes
Exclusions from above levels
Child codes
Sibling codes
AB50– Congenital hearing impairmentAB52– Deafness not otherwise specifiedAB53– Ototoxic hearing lossAB54– PresbycusisAB55– Sudden idiopathic hearing lossAB56– Hereditary hearing lossAB57– Auditory synaptopathy or neuropathyAB5Y– Other specified disorders with hearing impairmentAB5Z– Disorders with hearing impairment, unspecified
Foundation entity
Acquired hearing impairment – http://id.who.int/icd/entity/500439897
Allowed postcoordination axes
Part of: 10: Diseases of the ear or mastoid process