Jalili Syndrome C3495589
Jalili Syndrome is a rare genetic condition combining an inherited eye disease causing vision loss with a tooth enamel disorder. Ophthalmologists and dentists provide coordinated care for affected individuals.
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
Visual loss
Optic nerve atrophy
Generalized symptoms
(ophthalmologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Photophobia
(ophthalmologic)Retinal pigmentary changes
(ophthalmologic)Medication Comparisons
Compare medications used to treat Jalili Syndrome C3495589. 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.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy