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| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Mayo Clinic Laboratories Mayo Clinic United States | 7 | 1 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 5 | 3 |
|
Porphobilinogen, QN, Random, U Mayo Clinic Laboratories Mayo Clinic United States | 3 | 1 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 4 | 1 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 5 | 0 |
|
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 | 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 |
|
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 |
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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 |
|
Coproporphyria, 121300, Autosomal dominant; HCP (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 |
|
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.