Filters
| Tests names and labs | Conditions | Genes and analytes | Methods |
|---|---|---|---|
Centogene AG - the Rare Disease Company Germany | 786 | 1205 |
|
Cardiomyopathy, dilated type 1N Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Limb-Girdle Muscular Dystrophy Panel Genetic Services Laboratory University of Chicago United States | 46 | 31 |
|
Mayo Clinic Genetic Testing Laboratories Mayo CLinic United States | 1 | 77 |
|
Cardiomyopathies General Panel Health in Code Spain | 1 | 173 |
|
Hypertrophic cardiomyopathy extended panel Health in Code Spain | 1 | 104 |
|
Health in Code Spain | 1 | 218 |
|
Health in Code Spain | 1 | 57 |
|
Cardiovascular Diseases_General Panel Health in Code Spain | 1 | 380 |
|
Genetic Services Laboratory University of Chicago United States | 119 | 111 |
|
Hypertrophic Cardiomyopathy Extended Panel Health in Code Spain | 1 | 90 |
|
Health in Code Spain | 1 | 149 |
|
Ventricular Arrythmia & Sudden Death Panel with Structural Heart Disease Health in Code Spain | 1 | 141 |
|
Health in Code Spain | 1 | 46 |
|
Health in Code Spain | 1 | 81 |
|
Inherited Cardiovascular Diseases and Sudden Death Panel Health in Code Spain | 1 | 213 |
|
Limb-Girdle Muscular Dystrophy, autosomal recessive type 2G Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Limb-girdle muscular dystrophy panel Centogene AG - the Rare Disease Company Germany | 1 | 21 |
|
Genetic Study of Hypertrophic Cardiomyopathy Panel (2 panels: 57 genes or 18 genes) HeartGenetics, Genetics and Biotechnology, SA Portugal | 1 | 17 |
|
Pan Cardiomyopathy Panel (62 Genes) Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine United States | 103 | 61 |
|
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.