Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Lysosomal Diseases Testing Laboratory Thomas Jefferson University United States | 57 | 18 |
|
Lysosomal storage disorder by enzyme study from amniotic fluid and CVS Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 24 | 23 |
|
Cherry red spot and Neuroregression panel Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 7 | 6 |
|
Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 6 | 6 |
|
Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
|
Lysosomal Storage Disease Panel Molecular Genetics Laboratory London Health Sciences Centre Canada | 77 | 50 |
|
Centogene AG - the Rare Disease Company Germany | 195 | 221 |
|
CentoXome MOx (Whole Exome Sequencing) Centogene AG - the Rare Disease Company Germany | 13 | 19 |
|
Centogene AG - the Rare Disease Company Germany | 316 | 314 |
|
Centogene AG - the Rare Disease Company Germany | 12 | 18 |
|
Centogene AG - the Rare Disease Company Germany | 12 | 36 |
|
Centogene AG - the Rare Disease Company Germany | 10 | 10 |
|
Centogene AG - the Rare Disease Company Germany | 10 | 20 |
|
HEXB - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Carrier Screening Guidelines-Based Panel Ambry Genetics United States | 199 | 164 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 734 | 744 |
|
Centogene AG - the Rare Disease Company Germany | 669 | 688 |
|
Ataxia / Spastic Paraplegia Comprehensive Panel Centogene AG - the Rare Disease Company Germany | 451 | 452 |
|
Ataxia / Spastic Paraplegia Panel Centogene AG - the Rare Disease Company Germany | 442 | 443 |
|
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