Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
GeneDx United States | 1 | 1501 |
|
GeneDx United States | 19 | 293 |
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Mitochondrial Panel, Nuclear genes CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 145 | 134 |
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NewbornDx Advanced Sequencing Evaluation Athena Diagnostics United States | 1 | 1722 |
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Mitochondrial complex I deficiency, nuclear type: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 33 | 33 |
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Fulgent Genetics United States | 163 | 75 |
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Oxidative Phosphorylation Disorders NGS Panel Fulgent Genetics United States | 416 | 235 |
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Mental retardation - different panels Institute of Human Genetics Cologne University Germany | 7 | 2536 |
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MITOCHONDRIAL COMPLEX 1 DEFICIENCY (NUCLEAR GENE) Laboratorio de Genetica Clinica SL Spain | 1 | 18 |
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Neurogenetic Disorders - panels MGZ Medical Genetics Center Germany | 14 | 597 |
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Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University United States | 4 | 55 |
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Nuclear encoded Mitochondriopathies Panel CeGaT GmbH Germany | 37 | 302 |
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MGZ Medical Genetics Center Germany | 3 | 26 |
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MGZ Medical Genetics Center Germany | 6 | 168 |
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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 |
|
Fulgent Genetics United States | 5129 | 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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Mitochondrial Respiratory Chain Complex I Deficiency (Nuclear Genes) MGZ Medical Genetics Center Germany | 1 | 17 |
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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.