Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Comprehensive Neuromuscular Panel Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University United States | 6 | 79 |
|
Epilepsy Comprehensive NGS Panel Fulgent Genetics United States | 729 | 398 |
|
Lymphedema NGS Multi-Gene Panel (36 Genes) Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center, Location AMC Netherlands | 3 | 36 |
|
Hildebrandt Laboratory Boston Children's Hospital United States | 2 | 204 |
|
Congenital disorder of glycosylation type Ia Bioarray Spain | 1 | 1 |
|
CeGaT GmbH Germany | 1 | 1 |
|
Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 86 | 87 |
|
Congenital Disorders of Glycosylation (CDG) Panel CeGaT GmbH Germany | 20 | 34 |
|
Ataxia and differential diagnoses Panel CeGaT GmbH Germany | 173 | 204 |
|
Congenital Disorders of Glycosylation (CDG) Panel CeGaT GmbH Germany | 20 | 34 |
|
Congenital Disorders of Glycosylation (CDG) MGZ Medical Genetics Center Germany | 4 | 38 |
|
Fulgent Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 5129 | 4672 |
|
Fulgent Genetics United States | 1103 | 676 |
|
Fulgent Genetics United States | 259 | 112 |
|
Intellectual Disability NGS Panel Fulgent Genetics United States | 1058 | 554 |
|
Fulgent Genetics United States | 41 | 21 |
|
Congenital Disorders of Glycosylation NGS Panel Fulgent Genetics United States | 43 | 39 |
|
Congenital Disorders of Glycosylation Sequential Panel 1 FirmaLab United States | 1 | 4 |
|
Genome Diagnostics Laboratory University Medical Center Utrecht Netherlands | 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.