Nonsyndromic Deafness Y Linked Cn262180
Hearing loss inherited through genes on the Y chromosome, causing reduced hearing ability. It affects males and is passed from father to son. Hearing aids or other devices can help improve communication.
Key facts at a glance
- ICD-10
- Q17.9
- ICD-11
- LA00.0
- Body system
- otolaryngologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(otolaryngologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Prelingual sensorineural hearing loss
(otolaryngologic)Progressive sensorineural hearing loss
(otolaryngologic)Tinnitus
(otolaryngologic)Vestibular dysfunction
(otolaryngologic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Cochlear Implantation
Surgical placement of a cochlear implant device to provide direct electrical stimulation of the auditory nerve, enabling perception of sound in individuals with severe to profound hearing loss.
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Sign Language Communication Training
Comprehensive instruction in sign language and visual communication modalities to establish effective communication abilities and prevent language deprivation.
Additional treatment options
Hearing Aid Amplification
Provision and optimization of appropriately fitted hearing aids or amplification devices to maximize residual hearing capabilities.
procedureAssistive Technology Integration
Implementation of assistive listening devices, visual alert systems, and communication apps to enhance daily functioning and safety.
lifestyleWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Nonsyndromic Deafness Y Linked Cn262180?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Morton CC, Nance WE. Newborn hearing screening—a silent revolution. N Engl J Med. 2016.
Sheffield AM, Smith RJH. The molecular genetics of non-syndromic hearing loss. Curr Opin Otolaryngol Head Neck Surg. 2019.
Shi L, Guo L, Li K, Zhang Q. Identification of pathogenic variants in Chinese families with hereditary hearing loss. J Transl Med. 2020.
Van Camp G, Smith RJH. Hereditary Hearing Loss: A Comprehensive Reference. Hum Genet. 2022.
Medication Comparisons
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View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy