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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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Comprehensive Metabolism NGS Panel Fulgent Genetics United States | 602 | 355 |
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Fulgent Genetics United States | 121 | 23 |
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Fulgent Genetics United States | 39 | 27 |
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Familial Hypomagnesemia , Panel Massive Sequencing (NGS) 14 Genes Reference Laboratory Genetics Spain | 16 | 14 |
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Bartter Syndrome and related disorders , Panel Massive Sequencing (NGS) 22 Genes Reference Laboratory Genetics Spain | 21 | 22 |
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HYPOMAGNESEMIA, PRIMARY WITH HYPOCALCURIA (AUTOSOMAL DOMINANT ) Laboratorio de Genetica Clinica SL Spain | 2 | 2 |
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Renal Hypomagnesemia Type 2 , Sequencing FXYD2 Gene Reference Laboratory Genetics Spain | 1 | 1 |
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Blueprint Genetics Finland | 8 | 19 |
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Fulgent Genetics United States | 1 | 1 |
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Fulgent Genetics United States | 5129 | 4672 |
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Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders 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.