Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Hereditary Degenerative Syndromes Panel CeGaT GmbH Germany | 28 | 49 |
|
Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel CeGaT GmbH Germany | 147 | 143 |
|
Neurodegeneration with Brain Iron Accumulation (NBIA) Panel CeGaT GmbH Germany | 3 | 13 |
|
MGZ Medical Genetics Center Germany | 17 | 212 |
|
Neurodegeneration with Brain Iron Accumulation (NBIA) MGZ Medical Genetics Center Germany | 1 | 12 |
|
Brain Malformations / Neuronal Migration Disorders MGZ Medical Genetics Center Germany | 2 | 266 |
|
Epilepsy and Mitochondrial Encephalopathy MGZ Medical Genetics Center Germany | 17 | 186 |
|
MGZ Medical Genetics Center Germany | 17 | 89 |
|
Fulgent Genetics United States | 2 | 1 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Fulgent Genetics United States | 1103 | 676 |
|
Mitochondrial-Membrane Protein-Associated Neurodegeneration (MPAN), c19orf12, Sequencing NBIA Testing Center Oregon Health & Science University United States | 1 | 1 |
|
Mitochondrial-Membrane Protein-Associated Neurodegeneration (MPAN), c19orf12 Sequencing Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University United States | 1 | 1 |
|
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.