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| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Invitae Congenital Disorders of Glycosylation Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 203 | 152 |
|
Invitae Comprehensive Neuromuscular Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 353 | 208 |
|
Congenital Muscular Dystrophy (CMD) Panel PreventionGenetics, part of Exact Sciences United States | 34 | 28 |
|
Dystroglycan-Related Congenital Muscular Dystrophy Panel PreventionGenetics, part of Exact Sciences United States | 22 | 18 |
|
MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
|
Congenital disorder of glycosylation type 1u (sequence analysis of DPM2 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Inherited Metabolic Disorders Panel Dhiti Omics Technologies Private Ltd India | 376 | 317 |
|
Panel of congenital disorders of glycosylation. NGS panel of 47 genes. Genologica Medica Spain | 55 | 47 |
|
Asper Biogene Asper Biogene LLC Estonia | 59 | 28 |
|
Congenital Disorders of Glycolysation Asper Biogene Asper Biogene LLC Estonia | 53 | 49 |
|
Congenital disorders of glycosylation, type I: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 26 | 26 |
|
Neuromuscular Disorders NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 233 | 144 |
|
Congenital Muscular Dystrophy Advanced Sequencing Evaluation Athena Diagnostics United States | 37 | 23 |
|
Congenital Disorders of Glycosylation (CDG) Panel CeGaT GmbH Germany | 20 | 34 |
|
Congenital Disorders of Glycosylation (CDG) Panel CeGaT GmbH Germany | 20 | 34 |
|
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.