Genetic tests

Full name Analytes Gene panels Disease Laboratory
Respiratory disorders (gene panel): non-CF bronchiectasis; pulmonary hypertension; interstitial lung disease Respiratory Disorders panel (137 genes) - Ugent Centrum Medische Genetica - UZ Gent
Arrhytmogenic cardiopathy Arrhytmogenic cardiopathy - UGent Centrum Medische Genetica - UZ Gent
Dilated cardiomyopathy Dilated cardiomyopathy - UGent Centrum Medische Genetica - UZ Gent
Supravalvular aortic stenosis ELN Centrum Medische Genetica - UZ Gent
Lipodystrophy and/or hyperinsulinism (gene panel) Lipodystrophy and/or hyperinsulinism (30 genes) - IPG Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Obesity (gene panel) Obesity - 13 genes - IPG Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Inherited Kidney Diseases (Gene Panel) Panel Nephro-ULG-V1 Centre de Génétique Humaine - CHU Sart-Tilman
Fertilisation failure-oocyte maturation arrest-embryonic arrest (gene panel) Subfertility, infertility and gamete malfunction - UGent Centrum Medische Genetica - UZ Gent
Li-Fraumeni syndrome TP53 Li-Fraumeni syndrome Centrum Menselijke Erfelijkheid - KUL
Dilated Cardiomyopathy (Gene panel) Dilated Cardiomyopathy (79 genes) - IPG Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Breast Cancer Trial BRCA1, BRCA2 Centrum Menselijke Erfelijkheid - KUL
Lymphoproliferative syndrome, X-linked (SH2D1A gene) / Duncan's disease SH2D1A X-linked lymphoproliferative disease, X-linked lymphoproliferative disease due to SH2D1A deficiency Centrum Menselijke Erfelijkheid - KUL
End-stage renal disease, ESRD (gene panel) End-stage renal disease (106 genes) - IPG Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Nephrocalcinosis and nephrolithiasis (gene panel) Nephrocalcinosis and nephrolithiasis (37 genes) - IPG Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Parathyroid tumor (gene panel) CASR, CDC73, MEN1, RET Parathyroid tumor (4 genes) - KUL Neonatal severe primary hyperparathyroidism, Familial hypocalciuric hypercalcemia type 1, Autosomal dominant hypocalcemia Centrum Menselijke Erfelijkheid - KUL
41 pharmacogenes analysis pharmacogenes analysis Centre de Génétique Médicale UCL
Lymphoproliferative syndrome, X-linked (XIAP gene) XIAP X-linked lymphoproliferative disease, X-linked lymphoproliferative disease due to XIAP deficiency Centrum Menselijke Erfelijkheid - KUL
Myopia (early onset high myopia) Myopia gene panel - UGent Centrum Medische Genetica - UZ Gent
Craniosynostosis (gene panel) Craniosynostosis (UZ Gent) Centrum Medische Genetica - UZ Gent
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