Disorders

Hyperoxaluria, Primary, Type 3

Synonym(s): Primary Hyperoxaluria Type III

Gene	Locus	Protein
HOGA1	10q24.1	Serine--pyruvate aminotransferase

Laboratory	Test Method	Prenatal	Carrier *
Centre de Biologie Est - Hospices Civils de Lyon, Maladies hrditaires du mtabolisme - Bron cedex, France	• Analyte
Cologne University, Institute of Human Genetics - Cologne, Germany
UCL Hospitals, Clinical Biochemistry Laboratory - London, Great Britain

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.