Primary hyperoxaluria type 3

Primary hyperoxaluria type 3

Definition

Primary hyperoxaluria type 3 (PH3) is a disorder of glyoxylate metabolism that can be asymptomatic or characterized by oxalate nephrolithiasis.

Also known as HOGA1 primary hyperoxaluria, primary hyperoxaluria caused by mutation in HOGA1, primary hyperoxaluria type III — per MONDO

Also identified as