Reference |
Disease |
|---|---|
| SEQ1637 | Fanconi anemia |
| SEQ1065 | Familial Colorectal Cancer |
| SEQ1067 | Familial Endometrial Cancer |
| SEQ1357 | Bone and Soft Tissue Cancer (Sarcoma and Osteosarcoma) |
| SEQ1052 | Familial breast / ovarian cancer |
| SEQ1070 | Ovarian Cancer |
| SEQ1358 | Hereditary skin cancer |
| SEQ1055 | Familial Prostate Cancer |
| SEQ1355 | Central nervous system cancer |
| SEQ1354 | Cancer of the nervous / brain system (glioma) |
| SEQ1069 | Extended Familial Endocrine Cancer |
| SEQ1053 | Familial gastric cancer |
| SEQ1066 | Familial Pancreatic Cancer |
| SEQ1058 | Familial Parathyroid Cancer |
| SEQ1054 | Familial kidney cancer |
| SEQ1057 | Familial Thyroid Cancer |
| SEQ1345 | Familial non-medullary thyroid cancer |
| SEQ1064 | Familial Chondrosarcoma |
| EXN1040/SEQ1350 | Congenital Blackfan-Diamond Erythorblastopenia and Differential Diagnosis |
| SEQ1060 | Familial Pheochromocytoma |
| SEQ1063 | Familial Melanoma |
| SEQ1056 | Familial Multiple Endocrine Neoplasia |
| SEQ1081 | FAMILIAL BREAST/OVARIAN CANCER |
| SEQ1343 | Familial adenomatous polyposis |
| SEQ1344 | Juvenile polyposis |
| SEQ1348 | Predisposition to pediatric hematitis |
| EXN1149/SEQ1347 | Predisposition to myeloid pathologies |
| SEQ1359 | Predisposition to pediatric solid tumors |
| SEQ1360 | Predisposition to expanded cancer, multiple types |
| SEQ1049 | Predisposition to cancer, multiple types |
| EXN1120/SEQ1349 | Hereditary syndromes with bone marrow failure |
| SEQ1346 | Wilms tumor |
| SEQ references correspond to studies performed using NIMSeq® | |
| EXN references correspond to studies performed using ExoNIM® | |
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