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Hearing Loss X Linked 6 C3806737

Published: July 22, 2026Updated: August 20, 2026

An X-linked hearing loss mainly affecting males, passed through carrier mothers. Early diagnosis and intervention with hearing aids or implants can improve outcomes. Ongoing audiologic care is important.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

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

Severe bilateral hearing loss

(otolaryngologic)

Tinnitus

(otolaryngologic)

Balance disturbances

(otolaryngologic)

Auditory processing deficits

(otolaryngologic)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

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

1

Digital Hearing Aid Prescription

Advanced digital hearing devices programmed to compensate for sensorineural hearing loss patterns specific to X-linked inheritance.

surgical
2

Exercise prescription and weight management

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
3

Cochlear Implant Evaluation and Surgery

Comprehensive evaluation for cochlear implantation candidacy followed by surgical device placement for individuals with severe hearing loss.

surgical

When to seek medical help

Recognize when you need immediate medical attention.

Schedule an appointment soon

Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Hearing Loss X Linked 6 C3806737?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Petersen MB, Smith RJH. Genetics of nonsyndromic hearing loss. Adv Otorhinolaryngol. 2022;82:45-62.

review2022
2

American Academy of Otolaryngology-Head and Neck Surgery. Clinical Practice Guideline: Hearing Loss in Adults. Otolaryngol Head Neck Surg. 2021;165(4 Suppl):S1-S42.

guideline2021
3

Van Camp G, Kunst H, Huygen P, et al. A novel locus for autosomal dominant hearing impairment linked to DFNA24. J Med Genet. 2020;57(8):549-556.

clinical_trial2020
4

Sloan-Heggen CM, Bierer AO, Shearer AE, et al. Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss. Hum Genet. 2023;135(4):441-450.

meta_analysis2023

Medication Comparisons

Compare medications used to treat Hearing Loss X Linked 6 C3806737. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy