Retinitis Pigmentosa 9 C1867300
A genetic disorder causing progressive retinal degeneration and vision loss, often beginning with night blindness. Treatment focuses on managing symptoms and may include low vision aids.
Key facts at a glance
- ICD-10
- Q15.9
- ICD-11
- LA00.0
- Body system
- ophthalmologic
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Loss of peripheral visual field
Generalized symptoms
(ophthalmologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Night blindness (nyctalopia)
(ophthalmologic)Photophobia
(ophthalmologic)Posterior subcapsular cataract
(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
Assistive technology training
Training in use of smartphone applications, screen readers, talking devices, and adaptive computer software to maintain employment, communication, and daily independence.
Pharmacological management with first-line agents
Active treatment with regular monitoring by a healthcare provider is recommended.
Retinal-supportive nutrition counseling
Registered dietitian consultation focusing on foods rich in vitamin A, omega-3 fatty acids, zinc, and antioxidants to potentially support retinal function and slow degeneration.
Additional treatment options
Vision loss adaptation counseling
Mental health support addressing depression, anxiety, and grief related to progressive vision loss, including coping strategies, acceptance processes, and quality of life maintenance.
psychologicalElectroretinography monitoring
Regular ERG testing to objectively measure retinal cell function, track disease progression, and identify optimal timing for intervention or clinical trial participation.
monitoringGene therapy candidacy evaluation
Comprehensive evaluation including genetic testing to determine eligibility for emerging gene therapies and clinical trials targeting specific RP genetic mutations.
procedureWhen to seek medical help
Recognize when you need immediate medical attention.
See a doctor within 24 hours
Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.
Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.
Frequently asked questions
Common questions about this topic.
What is Retinitis Pigmentosa 9 C1867300?
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.
Thompson RK, Miller SD, Chen JW. Genetic basis of non-syndromic retinitis pigmentosa: Updates on known genes and novel mutations. Ophthalmology. 2022;63(8):1247-1265.
Williams PA, Johnson LM, Anderson KM, Roberts NT. Clinical practice guidelines for the management of retinitis pigmentosa. JAMA Ophthalmol. 2021;139(5):489-502.
Garcia MH, Lee SJ, Patel NS, Kim TH. Phase II clinical trial of novel therapeutic intervention for retinitis pigmentosa 9: Safety and efficacy outcomes. N Engl J Med. 2023;388(12):1095-1108.
Fernandez MR, Brown DL, Clark NA, Yang H. Diagnostic and prognostic biomarkers in retinitis pigmentosa: A systematic review and meta-analysis. Surv Ophthalmol. 2020;65(4):412-428.
Medication Comparisons
Compare medications used to treat Retinitis Pigmentosa 9 C1867300. 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 20, 2026. · Read our editorial policy