Disorders

Familial Juvenile Hyperuricemic Nephropathy Type 2

Synonym(s): Early-Onset Hyperuricemia, Anemia, and Progressive Tubulointerstitial Nephropathy, FJHN2, HNFJ2

Gene	Locus	Protein
REN	1q32	Renin

Laboratory	Test Method	Prenatal	Carrier *
Aachen, RWTH, Institute of Human Genetics - Aachen, Germany	• Linkage analysis
Center for Nephrology and Metabolic Disorders, Laboratory for Molecular Diagnostics - Weisswasser, Germany
Cologne University, Institute of Human Genetics - Cologne, Germany
General University Hospital in Prague, Institute of Inherited Metabolic Disorders - Praha, Czech Republic
Oxford Medical Genetics Laboratories, Oxford Genetics Laboratories - Oxford, 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.