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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
GeneDx United States | 1 | 1040 |
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Two Known Familial Variants in a Nuclear Gene GeneDx United States | 1 | 1043 |
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One Known Familial Variant in a Nuclear Gene GeneDx United States | 1 | 1045 |
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Fulgent Genetics United States | 1 | 1 |
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Rhabdomyolysis & Metabolic Myopathies NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 46 | 47 |
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Neurogenetic Disorders - panels MGZ Medical Genetics Center Germany | 14 | 597 |
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Nuclear encoded Mitochondriopathies Panel CeGaT GmbH Germany | 37 | 302 |
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Muscle Weakness (Myopathy, Muscular Dystrophy) MGZ Medical Genetics Center Germany | 6 | 179 |
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MGZ Medical Genetics Center Germany | 2 | 15 |
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MGZ Medical Genetics Center Germany | 6 | 168 |
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Metabolic Myopathy / Fatty Acid Oxidation Disorder / Myalgia / Rhabdomyolysis MGZ Medical Genetics Center Germany | 5 | 28 |
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Mitochondrial Diseases (mtDNA and 217 nuclear genes) Asper Biogene Asper Biogene LLC Estonia | 89 | 210 |
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Fulgent Genetics United States | 1103 | 676 |
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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.