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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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DYSF - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
|
Invitae Rhabdomyolysis and Metabolic Myopathy Panel Invitae United States | 202 | 128 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital United States | 480 | 254 |
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Invitae Comprehensive Carrier Screen Invitae United States | 886 | 547 |
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Metabolic Myopathies, Rhabdomyolysis and Exercise Intolerance Panel PreventionGenetics, part of Exact Sciences United States | 106 | 83 |
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Comprehensive Neuromuscular Panel PreventionGenetics, part of Exact Sciences United States | 183 | 142 |
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Invitae Comprehensive Muscular Dystrophy Panel Invitae United States | 114 | 52 |
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Invitae Limb-Girdle Muscular Dystrophy Panel Invitae United States | 91 | 37 |
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Invitae Comprehensive Myopathy Panel Invitae United States | 143 | 70 |
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Invitae Comprehensive Neuromuscular Disorders Panel Invitae United States | 353 | 208 |
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Limb Girdle Muscular Dystrophy Type 2B and Miyoshi Myopathy via the DYSF Gene PreventionGenetics, part of Exact Sciences United States | 3 | 1 |
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Inherited Neuromuscular Disorders Panel Dhiti Omics Technologies Private Ltd India | 16 | 7 |
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Congenital muscular dystrophy and LGMD panel. 42-gene NGS panel. Genologica Medica Spain | 96 | 42 |
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Metabolic myopathy and rhabdomyolysis panel. NGS panel of 52 genes. Genologica Medica Spain | 89 | 52 |
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Girdle muscular dystrophy. NGS panel of 39 genes. Genologica Medica Spain | 84 | 39 |
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Neuromuscular Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 138 | 62 |
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