Genetic tests

Full name Analytes Gene panels Disease Laboratory
Nephrogenetics / Nephropathy (gene panel) Nephropathy panel - UGent Centrum Medische Genetica - UZ Gent
Catecholaminergic polymorphic ventricular tachycardia (CPVT) Catecholaminergic polymorphic ventricular tachycardia (CPVT) - UGent Catecholaminergic polymorphic ventricular tachycardia Centrum Medische Genetica - UZ Gent
Dihydropyrimidine dehydrogenase deficiency; 5-fluorouracil toxicity - pharmacogenetics (4 variants: DPYD*2A, DPYD*13, c.2846A>T, HapB3) - Pharmacogenetics DPYD Dihydropyrimidine dehydrogenase deficiency Centrum Medische Genetica - UZ Gent
Renal cell carcinoma (kidney cancer) (gene panel) Renal cell carcinoma - UGent Centrum Medische Genetica - UZ Gent
Pancreatic cancer, familial (gene panel) Familial pancreatic cancer Centrum Medische Genetica - UZ Gent
Dicer1 tumor predisposition syndrome DICER1 Familial multinodular goiter, DICER1 tumor-predisposition syndrome, Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome, Malignant Sertoli-Leydig cell tumor of the ovary, Maligant granulosa cell tumor of the ovary, Gynandroblastoma Centrum Medische Genetica - UZ Gent
Microsatellites instability analysis- MMR genes MLH1, MSH2, MSH6, PMS2 Lynch syndrome, Constitutional mismatch repair deficiency syndrome Centre de Génétique Humaine - CHU Sart-Tilman
Lynch syndrome - MLH1 promoter hypermethylation and BRAF V600E mutation MLH1, BRAF Selection of therapeutic option in colorectal cancer Centre de Génétique Humaine - CHU Sart-Tilman
Breast and Ovarian Cancer, HBOC, Familial (12 genes) Breast/Ovarian cancer (12 genes) - IPG Hereditary breast and/or ovarian cancer syndrome Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Hirschsprung disease RET Hirschsprung disease Centre de Génétique Médicale UCL
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