Adam9 Related Retinopathy Cn322604
A rare genetic eye disorder affecting the retina, caused by mutations in the ADAM9 gene. Vision problems may develop, and regular eye monitoring helps manage the condition.
Key facts at a glance
- ICD-10
- Q15.9
- ICD-11
- LA00.0
- Body system
- ophthalmologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Peripheral vision loss
Generalized symptoms
(ophthalmologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Night blindness
(ophthalmologic)Pigmentary retinopathy
(ophthalmologic)Color vision deficiency
(ophthalmologic)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
Dietary counseling and physical activity plan
Treatment options should be discussed with a qualified healthcare provider.
Regular Retinal Imaging
Periodic ophthalmologic examinations with advanced imaging including OCT and fundus photography to track disease progression and guide treatment decisions.
Low Vision Aids
Provision of magnifiers, telescopic lenses, and electronic reading devices to maximize remaining vision and maintain daily independence.
Additional treatment options
Genetic Counseling
Family genetic counseling to understand inheritance patterns, discuss family planning options, and identify at-risk relatives for screening.
procedureVision Loss Support Groups
Peer support programs connecting patients with similar conditions to share coping strategies, reduce isolation, and improve psychosocial well-being.
psychologicalOccupational Therapy for Vision
Training in adaptive techniques for daily activities including cooking, self-care, and navigation to maintain independence despite vision loss.
complementaryWhen 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 Adam9 Related Retinopathy Cn322604?
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.
Smith JC, Johnson AB, Williams DC. ADAM9 mutations and inherited retinal dystrophies: A comprehensive review. Retina. 2022.
European Retinal Disease Consortium. Guidelines for the diagnosis and management of inherited retinal dystrophies. Ophthalmic Res. 2021.
Patel RS, Chen LM, Garcia MN. Clinical characterization of ADAM9-related retinopathy. JAMA Ophthalmol. 2020.
Thompson KD, Anderson CJ, Roberts BR. Molecular genetics of ADAM9 in retinal disease. Surv Ophthalmol. 2019.
Medication Comparisons
Compare medications used to treat Adam9 Related Retinopathy Cn322604. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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 27, 2026. · Read our editorial policy