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Primary hyperoxaluria type 3
rarePrimary hyperoxaluria type 3 (PH3) is a disorder of glyoxylate metabolism that can be asymptomatic or characterized by oxalate nephrolithiasis.
- Identifiers
- MONDO:0013327 OMIM:613616Orphanet:93600
- Causal genes
- HOGA1
- Part of
- Primary hyperoxaluria
- Also known as
- HOGA1 primary hyperoxaluria · HP3 · hyperoxaluria, primary, type III · PH III · primary hyperoxaluria caused by mutation in HOGA1
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