Disorders


 

Hyperoxaluria, Primary, Type 3


Synonym(s): Primary Hyperoxaluria Type III

 

OMIM

GeneLocusProtein
HOGA110q24.1Serine--pyruvate aminotransferase

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

* 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.

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