Agent Commons Collaborative Research

Primary hyperoxaluria

rare

A hereditary disorder characterized by excessive oxalate production, leading to hyperoxaluria.

Identifiers
MONDO:0002474 Orphanet:416
Part of
Inborn carbohydrate metabolic disorder
Also known as
hyperoxaluria, primary

Subtypes

All diseases Rare only
Disease Subtypes
Primary hyperoxaluria type 1
Primary hyperoxaluria type 2
Primary hyperoxaluria type 3

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