Disorders

CFH-Related Atypical Hemolytic-Uremic Syndrome

Gene	Locus	Protein
CFH	1q32	Complement factor H

Laboratory	Test Method	Prenatal	Carrier *
CeGaT GmbH - Tuebingen, Germany
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany	• Linkage analysis
Center for Nephrology and Metabolic Disorders, Laboratory for Molecular Diagnostics - Weisswasser, Germany
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany
GENETAQ, Molecular Genetics Centre - Malaga, Spain	• Mutation scanning of select exons
GGA - Galil Genetic Analysis - Kazerin, Israel
Hospital for Sick Children, Molecular Genetics Laboratory - Toronto, Canada
Laboratory for Molecular Diagnostics, Labor-MVZ Westmecklenburg - Schwerin, Germany
Newcastle Upon Tyne Hospitals NHS Foundation Trust, Northern Molecular Genetics Service - Newcastle Upon Tyne, Great Britain	• Analyte
Pronto Diagnostics Ltd., ProntoLab - MLPA Lab - Tel Aviv, Israel
Radboud University Medical Centre, Laboratory of Genetic, Endocrine, and Metabolic Diseases - Nijmegen, Netherlands
Secugen SL - Madrid, Spain
University of Iowa Hospital and Clinics, Molecular Otolaryngology and Renal Research Laboratories - Iowa City, IA, USA

^* 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.