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Other countries
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
ATPAF2 Sequence Analysis (Prenatal Diagnosis) Baylor Genetics United States | 1 | 1 |
|
ATPAF2 Deletion/Duplication Analysis Baylor Genetics United States | 1 | 1 |
|
ATPAF2 Comprehensive - Sequence & Deletion/Duplication Analysis Baylor Genetics United States | 1 | 1 |
|
Mitochondrial genome sequencing Molecular Vision Laboratory United States | 526 | 339 |
|
Mitochondrial Panel, Nuclear genes CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 145 | 134 |
|
Mitochondrial complex V (ATP synthase) deficiency, nuclear type: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 5 | 5 |
|
Oxidative Phosphorylation Disorders NGS Panel Fulgent Genetics United States | 416 | 235 |
|
Hyperammonemia and Urea Cycle Disorder NGS Panel Fulgent Genetics United States | 70 | 56 |
|
Epilepsy Comprehensive NGS Panel Fulgent Genetics United States | 729 | 398 |
|
Nuclear encoded Mitochondriopathies Panel CeGaT GmbH Germany | 37 | 302 |
|
MGZ Medical Genetics Center Germany | 3 | 4 |
|
Fulgent Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 5129 | 4672 |
|
Fulgent Genetics United States | 1103 | 676 |
|
Lactic Acidosis-Pyruvate NGS Panel Fulgent Genetics United States | 95 | 69 |
|
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.