Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Centogene AG - the Rare Disease Company Germany | 1 | 37 |
|
MT-TK Gene MERRF syndrome, MT-TK related NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 287 | 218 |
|
Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel Otogenetics United States | 123 | 129 |
|
Mitochondrial Genome Sequencing and Depletion/Integrity Panel Molecular Genetics Laboratory London Health Sciences Centre Canada | 48 | 52 |
|
Genomic Unity® Hearing Loss Disorders Analysis Variantyx, Inc. United States | 1 | 318 |
|
Mitochondrial Full Genome Analysis Mayo Clinic Laboratories Mayo Clinic United States | 29 | 37 |
|
Congenital Lactic Acidosis Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 65 |
|
PGmito - Mitochondrial Genome Sequencing PreventionGenetics, part of Exact Sciences United States | 16 | 38 |
|
Comprehensive Hearing Loss + mtDNA MNG Laboratories (Medical Neurogenetics, LLC.) United States | 218 | 300 |
|
Genomic Unity® Retinal Disorders Analysis Variantyx, Inc. United States | 1 | 394 |
|
CGC Genetics Unilabs Portugal | 1 | 837 |
|
Deafness or hypoacusis panel_v.2.0 CGC Genetics Unilabs Portugal | 1 | 272 |
|
MERRF syndrome (sequence analysis of A8344G mutation on MT-TK gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Sequence analysis of MT-TK gene CGC Genetics Unilabs Portugal | 1 | 1 |
|
Mitochondrial Diseases Panel (Nuclear and Mitochondrial DNA) Mendelics Brazil | 1 | 169 |
|
Dhiti Omics Technologies Private Ltd India | 28 | 37 |
|
MERRF Syndrome (A8344G, T8356C, G8363A and G8361A) Analysis Duzen Laboratories Duzen BBAGUAS Turkey | 1 | 1 |
|
Duzen Laboratories Duzen BBAGUAS Turkey | 1 | 1 |
|
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 1 | 37 |
|
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