Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Mayo Clinic Laboratories Mayo Clinic United States | 3 | 4 |
|
Department of Clinical Genetics Odense University Hospital Denmark | 1 | 1 |
|
Centogene US, LLC - The Rare Disease Company United States | 195 | 221 |
|
HMBS - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 1 | 1 |
|
Centogene US, LLC - The Rare Disease Company United States | 157 | 151 |
|
Centogene US, LLC - The Rare Disease Company United States | 669 | 688 |
|
Centogene US, LLC - The Rare Disease Company United States | 406 | 414 |
|
Centogene US, LLC - The Rare Disease Company United States | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 195 | 221 |
|
HMBS - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 669 | 688 |
|
Centogene AG - the Rare Disease Company Germany | 406 | 414 |
|
Centogene AG - the Rare Disease Company Germany | 157 | 151 |
|
Invitae Rhabdomyolysis and Metabolic Myopathy Panel Invitae United States | 202 | 128 |
|
Invitae Comprehensive Neurometabolic Disorders Panel Invitae United States | 351 | 249 |
|
Invitae Comprehensive Porphyrias Panel Invitae United States | 15 | 10 |
|
Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Porphyria, acute intermittent, 176000, Autosomal dominant (Acute intermittent porphyria) (MLPA) Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
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