Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Syndromic Hearing Loss NGS Panel Fulgent Genetics United States | 223 | 83 |
|
Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
|
Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics United States | 249 | 181 |
|
Quantitative Genomic Medicine Laboratories, SL Spain | 135 | 136 |
|
Molecular Vision Laboratory United States | 19 | 7 |
|
Hermansky-Pudlak Syndrome/Oculocutaneous Albinism/Pigmentation panel Molecular Vision Laboratory United States | 45 | 29 |
|
Fulgent Genetics United States | 4 | 1 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Craniofacial-deafness-hand syndrome MedGene Slovakia | 1 | 1 |
|
Waardenburg Syndrome NGS Panel Fulgent Genetics United States | 19 | 6 |
|
Fulgent Genetics United States | 52 | 28 |
|
Craniofacial-deafness-hand syndrome Praxis fuer Humangenetik Wien Austria | 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.