Filters
reset allOther countries
Results: 1 to 6 of 6
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Centogene AG - the Rare Disease Company Germany | 499 | 499 |
|
Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly Comprehensive Test HNL Genomics Connective Tissue Gene Tests United States | 1 | 1 |
|
Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly NGS Test HNL Genomics Connective Tissue Gene Tests United States | 1 | 1 |
|
Spondylo-Epi-Metaphyseal dysplasias NGS panel HNL Genomics Connective Tissue Gene Tests United States | 79 | 54 |
|
Spondylo-Epi-Metaphyseal dysplasias Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 79 | 54 |
|
Cleidocranial Dysplasia (CCD) via the RUNX2 Gene PreventionGenetics, part of Exact Sciences United States | 2 | 1 |
|
Results: 1 to 6 of 6
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.