Autosomal Recessive Nonsyndromic Hearing Loss 18a C1865870
Severe congenital hearing loss caused by genetic mutations passed from carrier parents. Present from birth, it affects hearing without other health problems. Treatment includes hearing aids, speech therapy, or cochlear implants.
Key facts at a glance
- ICD-10
- Q17.9
- ICD-11
- LA00.0
- Body system
- otolaryngologic
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(otolaryngologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Sensorineural hearing loss
(otolaryngologic)Tinnitus
(otolaryngologic)Difficulty understanding speech in noisy environments
(otolaryngologic)Ear fullness
(otolaryngologic)Medication Comparisons
Compare medications used to treat Autosomal Recessive Nonsyndromic Hearing Loss 18a C1865870. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy