Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Centogene AG - the Rare Disease Company Germany | 1 | 37 |
|
MT-TL1 Gene MELAS syndrome, MT-TL1 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 | 288 | 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 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
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 |
|
Epilepsy - Intellectual Disability - Autism Spectrum Disorder Amplexa Genetics Amplexa Genetics A/S Denmark | 1 | 600 |
|
Molecular Vision Laboratory United States | 342 | 268 |
|
Genomic Unity® Retinal Disorders Analysis Variantyx, Inc. United States | 1 | 394 |
|
CGC Genetics Unilabs Portugal | 1 | 837 |
|
MELAS syndrome (sequence analysis of MTTL1 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Mitochondrial dealfness (mutation T1095C, A1555G, A3243G, A7445G, 7472insC, T7510C and T7511C) CGC Genetics Unilabs Portugal | 1 | 3 |
|
Mitochondrial Diseases Panel (Nuclear and Mitochondrial DNA) Mendelics Brazil | 1 | 169 |
|
Dhiti Omics Technologies Private Ltd India | 28 | 37 |
|
Duzen Laboratories Duzen BBAGUAS Turkey | 1 | 1 |
|
Melas Syndrome (A3243G, T3271C, A3252G) Duzen Laboratories Duzen BBAGUAS Turkey | 1 | 1 |
|
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.