Primary hyperoxaluria type 3 (PH3) is a disorder of glyoxylate metabolism that can be asymptomatic or characterized by oxalate nephrolithiasis.
Comprehensive, easy-to-understand information about this condition
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Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.
AI-curated news mentioning primary hyperoxaluria type 3
Updated Jan 17, 2023
A family's journey highlights the emotional impact of their son's diagnosis of Primary Hyperoxaluria Type 1 (PH1). Their story emphasizes the importance of community support and awareness in navigating rare diseases.
A personal narrative highlights the challenges faced by individuals with Primary Hyperoxaluria Type 1 (PH1). The story emphasizes the emotional and physical toll of living with this rare disease, aiming to raise awareness and foster community support.