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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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CNBP - Repeat expansion analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Myotonic dystrophy 2, 602668, Autosomal dominant; DM2 (Proximal myotonic myopathy)(Repeat Analysis) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Variantyx, Inc. United States | 5 | 3 |
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Myotonic dystrophy type 2 (CCTG expansion on CNBP/ZNF9 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Molecular Genetics Laboratory BC Children's and BC Women's Hospitals Canada | 1 | 1 |
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Myotonic Dystrophy 2 (ZNF9/CNBP) Genetic Testing (Repeat Expansion) MNG Laboratories (Medical Neurogenetics, LLC.) United States | 1 | 1 |
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GeneDx United States | 1 | 1 |
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Myotonic dystrophy: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 2 | 2 |
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Myotonic Dystrophy Type 2 (CNBP) Repeat Expansion Fulgent Genetics United States | 1 | 1 |
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CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario Canada | 1 | 1 |
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Laboratorio de Genetica Clinica SL Spain | 1 | 0 |
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Myotonic Syndrome Advanced Evaluation Athena Diagnostics United States | 9 | 7 |
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Bioarray Spain | 1 | 1 |
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MVZ Dr. Eberhard & Partner Dortmund Germany | 1 | 1 |
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MVZ Dr. Eberhard & Partner Dortmund Germany | 1 | 1 |
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Fulgent Genetics United States | 1 | 1 |
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Athena Diagnostics United States | 1 | 1 |
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Fulgent Genetics United States | 5128 | 4672 |
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Praxis fuer Humangenetik Wien Austria | 1 | 1 |
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IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.