Any retinopathy caused by variants in the SPATA7 gene.
Comprehensive, easy-to-understand information about this condition
How we create this content →Connect with organizations supporting the SPATA7-related retinopathy community
Helpful links for rare disease information and support
Questions that may be helpful when speaking with your healthcare team
Connect with organizations supporting the SPATA7-related retinopathy community
Helpful links for rare disease information and support
Questions that may be helpful when speaking with your healthcare team
Connect with organizations supporting the SPATA7-related retinopathy community
Helpful links for rare disease information and support
Questions that may be helpful when speaking with your healthcare team
Patient Advocacy Groups (PAGs) provide support, resources, and community for patients and caregivers.
1 peer-reviewed source from PubMed
Common questions about SPATA7-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.