Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
ATP5A1 Sequence Analysis (Prenatal Diagnosis) Baylor Genetics United States | 1 | 1 |
|
GeneDx United States | 2 | 2592 |
|
GeneDx United States | 1 | 999 |
|
GeneDx United States | 1 | 1501 |
|
NewbornDx Advanced Sequencing Evaluation Athena Diagnostics United States | 1 | 1722 |
|
Combined oxidative phosphorylation deficiency: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 39 | 39 |
|
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 |
|
Fulgent Genetics United States | 1 | 1 |
|
Mental retardation - different panels Institute of Human Genetics Cologne University Germany | 7 | 2536 |
|
Neurogenetic Disorders - panels MGZ Medical Genetics Center Germany | 14 | 597 |
|
Nuclear encoded Mitochondriopathies Panel CeGaT GmbH Germany | 37 | 302 |
|
MGZ Medical Genetics Center Germany | 6 | 131 |
|
MGZ Medical Genetics Center Germany | 3 | 4 |
|
MGZ Medical Genetics Center Germany | 6 | 168 |
|
Mitochondrial Diseases (mtDNA and 217 nuclear genes) Asper Biogene Asper Biogene LLC Estonia | 89 | 210 |
|
Fulgent Genetics United States | 5129 | 4672 |
|
Fulgent Genetics United States | 1103 | 676 |
|
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