Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
EEF2 Gene Spinocerebellar ataxia type 26, autosomal dominant NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
CPOX Gene Coproporphyria NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 1 | 211 |
|
Peripheral Neuropathy Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 186 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 8 | 26 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 3 | 4 |
|
Centogene AG - the Rare Disease Company Germany | 195 | 205 |
|
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 Comprehensive Neurometabolic Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 351 | 249 |
|
Porphyria Comprehensive Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 11 |
|
Invitae Comprehensive Porphyrias Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 15 | 10 |
|
Harderoporphyria, 121300, Autosomal dominant (Hereditary coproporphyria) (Prenatal) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Harderoporphyria, 121300, Autosomal dominant (Hereditary coproporphyria) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Coproporphyria, 121300, Autosomal dominant; HCP (Hereditary coproporphyria) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 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.