Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
SmartMeds+ Pharmacogenomic Testing By Innovative GX Health Innovative Genomics InnovativeGx Health United States | 1 | 67 |
|
Centogene AG - the Rare Disease Company Germany | 1 | 37 |
|
MT-RNR1 Gene Deafness, nonsyndromic, sensorineural, mitochondrial 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 |
|
Genomic Unity® Hearing Loss Disorders Analysis Variantyx, Inc. United States | 1 | 318 |
|
AudioloGene Hearing Loss Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 200 |
|
PGx-Premium (Preemptive PGx test) SPMED CO., LTD Step forward Personalized Medicine South Korea | 66 | 27 |
|
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 |
|
Ariel Precision Medicine United States | 1 | 26 |
|
PGmito - Mitochondrial Genome Sequencing PreventionGenetics, part of Exact Sciences United States | 16 | 38 |
|
Genomic Unity® Retinal Disorders Analysis Variantyx, Inc. United States | 1 | 394 |
|
CGC Genetics Unilabs Portugal | 1 | 837 |
|
Mitochondrial dealfness (mutation T1095C, A1555G, A3243G, A7445G, 7472insC, T7510C and T7511C) CGC Genetics Unilabs Portugal | 1 | 3 |
|
Deafness nonsyndromic sensorineural mitochondrial (sequence analysis of MT-RNR1 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Dhiti Omics Technologies Private Ltd India | 28 | 37 |
|
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 1 | 37 |
|
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 1 | 37 |
|
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 1 | 37 |
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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.