AB33ICD-11 MMS 2026-01
Otosclerosis
Description
Otosclerosis is a genetically mediated metabolic bone disease that affects the otic capsule and stapes. It is an autosomal dominant disorder with varying penetrance and expressivity. Usually symptomatic hearing loss from otosclerosis develops early in the third decade of life, although onset in the teenage years does occur.
Index terms
- Otosclerosis
- otospongiosis
- Otosclerosis involving oval window, nonobliterative
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- nonobliterative otosclerosis
- Otosclerosis involving oval window, obliterative
- obliterative otosclerosis
- Cochlear otosclerosis
- Otosclerosis involving round window
- Otosclerosis involving otic capsule
Inclusions
- otospongiosis
Exclusions from above levels
Sibling codes
AB30– Acute vestibular syndromeAB31– Episodic vestibular syndromeAB32– Chronic vestibular syndromeAB34– Disorders of vestibular functionAB35– Labyrinthine fistulaAB36– Labyrinthine dysfunctionAB37– Noise effects on inner earAB3Y– Other specified diseases of inner earAB3Z– Diseases of inner ear, unspecified
Foundation entity
Allowed postcoordination axes
Part of: 10: Diseases of the ear or mastoid process