Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
NGLY1 - Congenital disorder of glycosylation type IV Translational Metabolic Laboratory Radboud University Medical Centre Netherlands | 1 | 1 |
|
Congenital Disorders of Glycosylation (CDG) Panel PreventionGenetics, part of Exact Sciences United States | 56 | 54 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 466 | 297 |
|
Invitae Congenital Disorders of Glycosylation Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 203 | 152 |
|
Early Infantile Epileptic Encephalopathy Panel PreventionGenetics, part of Exact Sciences United States | 144 | 124 |
|
Baylor Genetics United States | 1 | 397 |
|
Neurodevelopmental Disorders Panel Baylor Genetics United States | 1 | 236 |
|
Cerebral Palsy Spectrum Disorders Panel Baylor Genetics United States | 1 | 419 |
|
MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
|
Hereditary ataxias panel_v.2.0 CGC Genetics Unilabs Portugal | 1 | 427 |
|
Nuclear-Encoded Mitochondrial Disorders Panel CGC Genetics Unilabs Portugal | 1 | 306 |
|
CGC Genetics Unilabs Portugal | 1 | 837 |
|
Movement diseases (WES based NGS panel of 931 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 10 | 930 |
|
CGC Genetics Unilabs Portugal | 1 | 759 |
|
CGC Genetics Unilabs Portugal | 1 | 1307 |
|
Parkinson's and movement disorders panel_v.2.0 CGC Genetics Unilabs Portugal | 1 | 256 |
|
Comprehensive Epilepsy Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 234 | 240 |
|
Congenital disorders of glycosylation (WES based NGS panel of 39 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 39 |
|
Congenital disorder of glycosylation type 1v (sequence analysis of NGLY1 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Integrated Genetics Westborough LabCorp United States | 330 | 746 |
|
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