Genetic tests

Full name Analytes Gene panels Disease Laboratory
Onco-endocrine pathologies (gene panel) Onco-endocine pathologies (50 genes) - UCL Centre de Génétique Médicale UCL
Myeloid/lymphoid neoplasms with germline predisposition Centre de Génétique Humaine - CHU Sart-Tilman
Erythrocytoses, polycythémies, thrombocytoses et neutropénies congénitales (gene panel) Erythocyoses, polycythémies, thrombocytoses congénitales (gene panel) - ULG Centre de Génétique Humaine - CHU Sart-Tilman
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
Neurodegeneration with Brain Iron Accumulation (gene panel) Neurodegeneration with Brain Iron Accumulation (NBIA) - UGent Centrum Medische Genetica - UZ Gent
TPMT*2,*3A, *3B, *3C, *3D, *4 - drug metabolism - Pharmacogenetics TPMT Centre de Génétique Médicale UCL
MTHFR c.677C>T et c.1298A>C -drug metabolism - Pharmacogenetics MTHFR Centre de Génétique Médicale UCL
Malignant Mesothelioma (BAP1; CDKN2A genes) BAP1, CDKN2A Centrum Menselijke Erfelijkheid - KUL
Test Cytogenetics analysis (BCR-ABL fusion gene ((t(9;22)) / Philadelphia chromosome) Sciensano
Microphthalmia / Anophthalmia / Coloboma-Anterior Segment Dysgenesis (MAC-ASD) (gene panel) Microphthalmia/Anophthalmia/Coloboma - Anterior Segment Dysgenesis - UGent Centrum Medische Genetica - UZ Gent
Rendu-Osler-Weber disease (4 genes) Rendu/Osler/weber (4 genes) - UCL, Vascular malformations (germline) (38 genes) - UCL Centre de Génétique Médicale UCL
test (α-D-galactosidase) Centre de Génétique Humaine - CHU Sart-Tilman
Resistance to clopidrogel - PON1 genotyping (Q192R) - Pharmacogenetics Centre de Génétique Médicale UCL
Dilated Cardiomyopathy (Gene panel) Dilated Cardiomyopathy (79 genes) - IPG Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Overgrowth & vascular anomalies (gene panel) Overgrowth & vascular anomalies (65 genes) - KUL Centrum Menselijke Erfelijkheid - KUL
Silver-Russell syndrome (11p15 methylation) Centrum Menselijke Erfelijkheid - KUL
Epilepsy without developmental delay, familial (gene panel) (Familial) epilepsy without developmental delay (gene panel) Centrum Medische Genetica - UZ Antwerpen
Breast Cancer Trial BRCA1, BRCA2 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)
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