An inherited retinopathy caused by bi-allelic variants in the GPR179 gene.
Comprehensive, easy-to-understand information about this condition
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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.