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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Homocystinuria caused by Cystathionine Beta-Synthase Deficiency, Sequencing MTR Gene Reference Laboratory Genetics Spain | 1 | 1 |
|
Methylmalonic Acidemia Sequencing NextGen Panel Children's Hospital Colorado Precision Diagnostics Laboratory Children's Hospital Colorado United States | 25 | 13 |
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ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 26 | 29 |
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Fulgent Genetics United States | 2 | 1 |
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Fulgent Genetics United States | 5129 | 4672 |
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Fulgent Genetics United States | 1103 | 676 |
|
Hyperhomocysteinemia due to Methionine synthase deficiency, cblG (MTR) Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD Netherlands | 1 | 1 |
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Intellectual Disability NGS Panel Fulgent Genetics United States | 1058 | 554 |
|
Cobalamin Homocysteine Methionine NGS Panel Fulgent Genetics United States | 23 | 20 |
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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.