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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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Developmental and epileptic encephalopathy: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 91 | 90 |
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Mitochondrial genome sequencing Molecular Vision Laboratory United States | 526 | 339 |
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Early Infantile Epileptic Encephalopathy NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 114 | 86 |
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Epileptic encephalopathy, early infantile: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 76 | 76 |
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Fulgent Genetics United States | 509 | 275 |
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Oxidative Phosphorylation Disorders NGS Panel Fulgent Genetics United States | 416 | 235 |
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Hypomyelinating Leukodystrophy NGS Panel Fulgent Genetics United States | 225 | 62 |
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EPILEPTIC ENCEPHALOPATHY WITH GLOBAL CEREBRAL DEMYELINATION Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
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Epilepsy Comprehensive NGS Panel Fulgent Genetics United States | 729 | 398 |
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Fulgent Genetics United States | 1 | 1 |
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Arginyl-tRNA synthetase deficiency, Hypomyelination due to (RARS) Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD Netherlands | 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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Intellectual Disability NGS Panel Fulgent Genetics United States | 1058 | 554 |
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Fulgent Genetics United States | 155 | 69 |
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Baylor Genetics United States | 842 | 637 |
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SLC25A12 - Global Cerebral Hypomyelination Centre for Inherited Metabolic Diseases Karolinska University Hospital Sweden | 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.