Primary hyperoxaluria

Definition

A disorder of glyoxylate metabolism characterized by an excess of oxalate resulting in kidney stones, nephrocalcinosis and ultimately renal failure and systemic oxalosis. There are 3 types of PH, types 1-3, all caused by liver-specific enzyme defects.

Disease data

Classification

Disease

ORPHA code

416

OMIM code

613616

ICD10 code

E74.8

ICD11 code

5C51.2Y

*Soruce