Primary hyperoxaluria type 3

MONDO:0013327

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, HP3, PH III, hyperoxaluria, primary, type 3, hyperoxaluria, primary, type III

2 clinical trials for this condition and its sub-types, 2 tagged with Primary hyperoxaluria type 3 itself.

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↑ Primary hyperoxaluria (17)

Including sub-types (2) Tagged with Primary hyperoxaluria type 3 (2)

Not yet finished but already full! 1 Completed 1

Newborn screening study aims to catch rare diseases at birth

Diagnosis Ongoing

This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

Sponsor: RTI International • Aim: Diagnosis

Last updated Jul 03, 2026 00:00 UTC

Primary hyperoxaluria type 3

Where it sits in the disease tree

Newborn screening study aims to catch rare diseases at birth