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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Invitae Rhabdomyolysis and Metabolic Myopathy Panel Invitae United States | 202 | 128 |
|
PreventionGenetics, part of Exact Sciences United States | 285 | 137 |
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Invitae Nuclear Mitochondrial Disorders Panel Invitae United States | 394 | 319 |
|
Mitochondrial Disorders Panel (Nuclear Genes Only) PreventionGenetics, part of Exact Sciences United States | 292 | 253 |
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Anterior Segment Dysgenesis Disorders Panel PreventionGenetics, part of Exact Sciences United States | 272 | 278 |
|
PreventionGenetics, part of Exact Sciences United States | 157 | 171 |
|
Metabolic Myopathies, Rhabdomyolysis and Exercise Intolerance Panel PreventionGenetics, part of Exact Sciences United States | 106 | 83 |
|
Invitae Organic Acidemias Panel Invitae United States | 108 | 97 |
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Invitae Comprehensive Neuromuscular Disorders Panel Invitae United States | 353 | 208 |
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Sengers Syndrome via the AGK Gene PreventionGenetics, part of Exact Sciences United States | 2 | 1 |
|
PreventionGenetics, part of Exact Sciences United States | 44 | 41 |
|
Mitochondrial Genome Maintenance/Integrity Nuclear Genes Panel PreventionGenetics, part of Exact Sciences United States | 27 | 22 |
|
Baylor Genetics United States | 842 | 637 |
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AGK Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 2 | 1 |
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Comprehensive Metabolism NGS Panel Fulgent Genetics United States | 602 | 355 |
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Congenital Cataracts NGS Panel Fulgent Genetics United States | 106 | 56 |
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Oxidative Phosphorylation Disorders NGS Panel Fulgent Genetics United States | 416 | 235 |
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MITOCHONDRIAL DNA DEPLETION SYNDROME, MYOPATHIC FORM Laboratorio de Genetica Clinica SL Spain | 2 | 2 |
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Invitae United States | 46 | 32 |
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AGK Gene Sequencing and Deletion/Duplication Analysis DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States | 2 | 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.