Disorders


 

Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome, PRKAG2-Related


 

OMIM

GeneLocusProtein
PRKAG27q35-q365'-AMP-activated protein kinase subunit gamma-2

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany  
Cincinnati Children's Hospital Medical Center, Heart Institute Diagnostic Lab - Cincinnati, OH, USA  
Correlagen Diagnostics, Inc. - Westborough, MA, USA  
GeneDx - Gaithersburg, MD, USA  
General University Hospital in Prague, Institute of Inherited Metabolic Disorders - Praha, Czech Republic  
GGA - Galil Genetic Analysis - Kazerin, Israel  
Groupe Hospitalier Pitié Salpêtrière, Molecular and Cellular Cardiogenetics and Myogenetics Unit - Paris, France  
Harvard Medical School and Partners Healthcare, Laboratory for Molecular Medicine - Cambridge, MA, USA  
Health in Code S.L. - A Coruña, Spain  
Oxford Medical Genetics Laboratories, Oxford Genetics Laboratories - Oxford, Great Britain  
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA  
Pronto Diagnostics Ltd., ProntoLab - MLPA Lab - Tel Aviv, Israel  
Transgenomic - New Haven, CT, USA  
University Hospital Münster, Institute for Genetics of Heart Diseases (IfGH) - Münster, Germany  

* 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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