Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Epilepsy Comprehensive NGS Panel Fulgent Genetics United States | 729 | 398 |
|
Leukodystrophy / Leukencephalopathy and differential diagnoses Panel CeGaT GmbH Germany | 69 | 175 |
|
Nuclear encoded Mitochondriopathies Panel CeGaT GmbH Germany | 37 | 284 |
|
MGZ Medical Genetics Center Germany | 3 | 26 |
|
MGZ Medical Genetics Center Germany | 17 | 212 |
|
MGZ Medical Genetics Center Germany | 6 | 131 |
|
MGZ Medical Genetics Center Germany | 6 | 168 |
|
Epilepsy and Mitochondrial Encephalopathy MGZ Medical Genetics Center Germany | 17 | 186 |
|
Fulgent Genetics United States | 2 | 1 |
|
Fulgent Genetics United States | 5130 | 4674 |
|
Fulgent Genetics United States | 1103 | 676 |
|
Lactic Acidosis-Pyruvate NGS Panel Fulgent Genetics United States | 129 | 69 |
|
Baylor Genetics United States | 842 | 637 |
|
Leigh Syndrome (nuclear DNA mutation) MGZ Medical Genetics Center Germany | 1 | 25 |
|
Mitochondrial Respiratory Chain Complex I Deficiency (Nuclear Genes) MGZ Medical Genetics Center Germany | 1 | 17 |
|
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.