Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Craniodysmorphology Panel (FGFR1,2,3,TWIST) Center for Genetics at Saint Francis Saint Francis Hospital United States | 8 | 4 |
|
Centogene AG - the Rare Disease Company Germany | 243 | 238 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 740 | 728 |
|
Congenital Diaphragmatic Hernia Panel PreventionGenetics, part of Exact Sciences United States | 116 | 65 |
|
Craniosynostosis core Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 5 |
|
Craniosynostosis Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 25 |
|
Craniosynostosis core Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 5 |
|
HNL Genomics Connective Tissue Gene Tests United States | 1 | 25 |
|
Craniosynostosis core NGS panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 5 |
|
Craniosynostosis Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 25 |
|
Polydactyly and Syndactyly Panel PreventionGenetics, part of Exact Sciences United States | 320 | 231 |
|
PreventionGenetics, part of Exact Sciences United States | 231 | 139 |
|
PreventionGenetics, part of Exact Sciences United States | 220 | 128 |
|
Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 110 | 45 |
|
qGenEx Intellectual disability Quantitative Genomic Medicine Laboratories, SL Spain | 3 | 1969 |
|
HNL Genomics Connective Tissue Gene Tests United States | 31 | 26 |
|
Craniosynostosis Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 31 | 26 |
|
Craniosynostosis Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 31 | 26 |
|
Craniosynostosis core Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 5 |
|
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.