Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Fulgent Genetics United States | 1 | 1 |
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mtDNA Targeted Analysis: Known Familial Mutation Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 11 | 34 |
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mtDNA Targeted Analysis with Heteroplasmy: Known Familial Mutation Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 11 | 34 |
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Expanded 93 mtDNA Variant Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 11 | 34 |
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Leber Hereditary Optic Neuropathy (LHON) Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile | 1 | 3 |
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Centogene AG - the Rare Disease Company Germany | 1 | 37 |
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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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MT-ND1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
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Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 287 | 218 |
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Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (MELAS) Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile | 1 | 3 |
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Mitochondrial DNA-Associated Leigh Syndrome and NARP Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile | 1 | 26 |
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Mitochondrial Non Syndromic Hearing Loss and Deafness Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile | 1 | 4 |
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Leber hereditary optic atrophy(LHON): 3 mutations(G3460A, G11778A, T14484C) Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 3 |
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Leber's Hereditary Optic Neuropathy Molecular Genetics Laboratory London Health Sciences Centre Canada | 1 | 3 |
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Genomic Unity® Hearing Loss Disorders Analysis Variantyx, Inc. United States | 1 | 318 |
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Molecular Vision Laboratory United States | 1358 | 1028 |
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Leber Hereditary Optic Neuropathy (LHON) - Targeted Testing for 3 Common Pathogenic Variants PreventionGenetics, part of Exact Sciences United States | 1 | 3 |
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Mitochondrial Full Genome Analysis Mayo Clinic Laboratories Mayo Clinic United States | 29 | 37 |
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Congenital Lactic Acidosis Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 65 |
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PGmito - Mitochondrial Genome Sequencing PreventionGenetics, part of Exact Sciences United States | 16 | 38 |
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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.