Disorders


 

TNNT2-Related Familial Hypertrophic Cardiomyopathy


 

OMIM

GeneLocusProtein
TNNT21q32Troponin T, cardiac muscle

Laboratory Test Method Prenatal Carrier *
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands  
Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany  
Centogene AG, Rare Disease Company - Rostock, Germany  
CGC Genetics - Porto, Portugal• Sequence analysis of select exons
  
Cincinnati Children's Hospital Medical Center, Heart Institute Diagnostic Lab - Cincinnati, OH, USA  
Correlagen Diagnostics, Inc. - Westborough, MA, USA  
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany  
Dr. Eberhard and Partner, MVZ Dortmund - Dortmund, Germany  
GeneDx - Gaithersburg, MD, USA  
GENETAQ, Molecular Genetics Centre - Malaga, Spain  
GGA - Galil Genetic Analysis - Kazerin, Israel  
Harvard Medical School and Partners Healthcare, Laboratory for Molecular Medicine - Cambridge, MA, USA  
Health Care Center GENOMED, Laboratory of Human Genetics - Warsaw, Poland• Sequence analysis of select exons
  
Health in Code S.L. - A Coruña, Spain  
InVitae Corporation - San Francisco, CA, USA  
Laboratory for Molecular Diagnostics, Labor-MVZ Westmecklenburg - Schwerin, Germany  
Maastricht University Medical Centre, Clinical Genomics - Maastricht, Netherlands  
Oslo University Hospital HF - Ullevaal, Department of Medical Genetics - Unit for Cardiac and Cardiavasular Genetics - Oslo, Norway  
Oxford Medical Genetics Laboratories, Oxford Genetics Laboratories - Oxford, Great Britain  
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA  
Transgenomic - New Haven, CT, USA  
University Hospital Münster, Institute for Genetics of Heart Diseases (IfGH) - Münster, Germany  
University of Goettingen, Institute of Human Genetics - Goettingen, 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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