Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
OPHTHALMOPLEGIA, PROGRESSIVE EXTERNAL (PEO) Laboratorio de Genetica Clinica SL Spain | 5 | 4 |
|
Neuromuscular Disorders NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 233 | 144 |
|
Mitochondrial Depletion NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 32 | 23 |
|
Rhabdomyolysis & Metabolic Myopathies NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 46 | 47 |
|
Asper Biogene Asper Biogene LLC Estonia | 180 | 139 |
|
Progressive external ophthalmoplegia, autosomal dominant, 3 Bioarray Spain | 1 | 1 |
|
CeGaT GmbH Germany | 3 | 1 |
|
Ataxia and differential diagnoses Panel CeGaT GmbH Germany | 173 | 204 |
|
Nuclear encoded Mitochondriopathies Panel CeGaT GmbH Germany | 37 | 284 |
|
TWINKLE (PEO1/C10orf2) DNA Sequencing Test (Related to mtDNA depletion) Athena Diagnostics United States | 2 | 1 |
|
Mitochondrial Hepatoencephalopathic Evaluation (POLG, DGUOK, MPV17, TWINKLE) Athena Diagnostics United States | 9 | 4 |
|
Baylor Genetics United States | 842 | 637 |
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Ophthalmoplegia, progressive external 3 MedGene Slovakia | 1 | 1 |
|
Ophthalmoplegia, progressive external 3 Praxis fuer Humangenetik Wien Austria | 1 | 1 |
|
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant 3 MGZ Medical Genetics Center Germany | 1 | 1 |
|
TWNK/C10orf2-Related Mitochondrial Disorder MGZ Medical Genetics Center Germany | 8 | 1 |
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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.