Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Ataxia and differential diagnoses Panel CeGaT GmbH Germany | 173 | 204 |
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Nuclear encoded Mitochondriopathies Panel CeGaT GmbH Germany | 37 | 284 |
|
CeGaT GmbH Germany | 7 | 8 |
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MGZ Medical Genetics Center Germany | 1 | 11 |
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MGZ Medical Genetics Center Germany | 6 | 131 |
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MGZ Medical Genetics Center Germany | 6 | 168 |
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Mitochondrial Encephalopathy / Leigh Syndrome – Basic Diagnostic MGZ Medical Genetics Center Germany | 6 | 33 |
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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 | 1 | 1 |
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Fulgent Genetics United States | 5128 | 4672 |
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Fulgent Genetics United States | 1103 | 676 |
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Lactic Acidosis-Pyruvate NGS Panel Fulgent Genetics United States | 95 | 69 |
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Baylor Genetics United States | 842 | 637 |
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COQ9-Related Coenzyme Q10 Deficiency MGZ Medical Genetics Center Germany | 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.