Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Mitochondrial Hearing Loss - MTTS1 Gene Center for Genetics at Saint Francis Saint Francis Hospital United States | 1 | 1 |
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Mitochondrial Hearing Loss - Mutation MT A1555G Center for Genetics at Saint Francis Saint Francis Hospital United States | 1 | 1 |
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Aminoglycoside-Induced Hearing Loss Panel Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 7 | 3 |
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Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 287 | 218 |
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Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel Otogenetics United States | 122 | 128 |
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Molecular Vision Laboratory United States | 1358 | 1028 |
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TRMU - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 406 | 414 |
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Centogene AG - the Rare Disease Company Germany | 498 | 498 |
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Centogene AG - the Rare Disease Company Germany | 499 | 499 |
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Centogene AG - the Rare Disease Company Germany | 203 | 194 |
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Centogene AG - the Rare Disease Company Germany | 829 | 848 |
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Invitae United States | 210 | 134 |
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Invitae Nuclear Mitochondrial Disorders Panel Invitae United States | 394 | 319 |
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PreventionGenetics, part of Exact Sciences United States | 130 | 69 |
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Mitochondrial Disorders Panel (Nuclear Genes Only) PreventionGenetics, part of Exact Sciences United States | 292 | 253 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Invitae Comprehensive Carrier Screen Invitae United States | 886 | 547 |
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TRMU - Combined oxidative phosphorylation deficiency Translational Metabolic Laboratory Radboud University Medical Centre Netherlands | 2 | 1 |
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