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Results: 1 to 8 of 8
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Fatty Acid Oxidation Probe Assay, Fibroblast Culture Mayo Clinic Laboratories Mayo Clinic United States | 7 | 1 |
|
Acylcarnitine Analysis - Plasma Baylor Genetics United States | 23 | 27 |
|
Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Clinical Biochemical Genetics Diagnostic Laboratory University Of Miami Miller School Of Medicine United States | 1 | 4 |
|
Trifunctional Protein Deficiency Clinical Biochemical Genetics Diagnostic Laboratory University Of Miami Miller School Of Medicine United States | 1 | 4 |
|
Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Dep. of Paediatrics and Inherited Metabolic Disorders General University Hospital in Prague and First Faculty of Medicine, Charles University in Prague Czech Republic | 1 | 1 |
|
Trifunctional Protein Deficiency Revvity Omics Revvity United States | 1 | 1 |
|
MTP deficiency (HADHA and HADHB genes) Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD Netherlands | 1 | 2 |
|
Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD Netherlands | 1 | 1 |
|
Results: 1 to 8 of 8
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.