A retinopathy caused by biallelic variants in the LCA5 gene.
Comprehensive, easy-to-understand information about this condition
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Questions that may be helpful when speaking with your healthcare team
Common questions about LCA5-related retinopathy
AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.