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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Inherited Metabolic Disorders Panel Dhiti Omics Technologies Private Ltd India | 376 | 317 |
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Metabolic myopathy and rhabdomyolysis panel. NGS panel of 52 genes. Genologica Medica Spain | 89 | 52 |
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Glycogen storage disorder panel. 29-gene NGS panel. Genologica Medica Spain | 33 | 29 |
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Hypoglycemia, hyperinsulinism, and ketone metabolism panel. NGS panel of 50 genes. Genologica Medica Spain | 73 | 50 |
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Glycogenosis (inherited metabolic disorders). NGS panel of 24 genes. Genologica Medica Spain | 30 | 24 |
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General panel of metabolic myopathies Genologica Medica Spain | 114 | 110 |
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Glycogen Storage Disorders Panel, Sequencing ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 40 | 32 |
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Glycogen Storage Diseases Gene Panel Duzen Laboratories Duzen BBAGUAS Turkey | 28 | 26 |
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LDHA Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States | 1 | 1 |
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Comprehensive Metabolism NGS Panel Fulgent Genetics United States | 602 | 355 |
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Fulgent Genetics United States | 36 | 30 |
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Congenital Myopathy , Panel Massive Sequencing (NGS) 26 Genes Reference Laboratory Genetics Spain | 24 | 26 |
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Metabolic Myopathy and Rhabdomyolysis Asper Biogene Asper Biogene LLC Estonia | 63 | 44 |
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Asper Biogene Asper Biogene LLC Estonia | 25 | 25 |
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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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CeGaT GmbH Germany | 26 | 44 |
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Fulgent Genetics United States | 1 | 1 |
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Fulgent Genetics United States | 5129 | 4672 |
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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.