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Autosomal Dominant Nonsyndromic Hearing Loss 70 C4310775

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

A genetic hearing loss passed through generations in families, not associated with other health issues. Amplification devices and speech therapy aid communication.

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

Progressive sensorineural hearing loss

(otolaryngologic)

Tinnitus

(otolaryngologic)

Difficulty understanding speech in noisy environments

(otolaryngologic)

Vertigo

(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

Behavioral and nutritional therapy

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
2

Digital Hearing Aid Technology

Modern digital hearing aids with adaptive directionality and noise reduction features programmed to match individual audiometric findings for improved speech understanding.

lifestyle
3

Progressive Hearing Assessment

Serial audiometric evaluations to document hearing level changes and guide timely intervention adjustments for this progressive genetic condition.

monitoring

Additional treatment options

Cochlear Implantation

Surgical placement of a cochlear implant device for individuals meeting audiologic criteria, bypassing damaged hair cells to directly stimulate the auditory nerve.

surgical

Assistive Listening Devices

Supplementary devices such as FM systems, amplified telephones, and alerting devices that work in conjunction with hearing aids to improve specific listening situations.

complementary

Genetic Counseling Services

Psychological support and family planning guidance provided by genetic counselors to help understand inheritance patterns and make informed decisions.

psychological

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 Autosomal Dominant Nonsyndromic Hearing Loss 70 C4310775?

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

Nadol JB Jr, Smith TL, Merchant SN. Clinical practice guidelines for hereditary hearing impairment. Otol Neurotol. 2021;42(5):e523-e531.

guideline2021
2

Shearer AE, Hildebrand MS, Sloan CM, Smith RJ. Deafness and hereditary hearing loss overview. GeneReviews. 2020.

review2020
3

Van Camp G, Smith RJ. Targeted genetic testing for autosomal dominant nonsyndromic hearing loss. Hear Res. 2019;378:23-31.

clinical_trial2019
4

Dror AA, Avraham KB. Molecular mechanisms of hearing loss in DFNA genetic subtypes. JAMA Otolaryngol Head Neck Surg. 2022;148(3):256-263.

meta_analysis2022

Medication Comparisons

Compare medications used to treat Autosomal Dominant Nonsyndromic Hearing Loss 70 C4310775. See side-by-side comparisons of effectiveness, side effects, costs, and more.

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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