Genetic tests

Full name Analytes Gene panels Disease Laboratory
Endocrine Disorders - Hypothyroidism (gene panel - 42 genes) Endocrine Disorders - Hypothyroidism (42 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Endocrine Disorders - Hyper(Hypo)parathyroidism (gene panel - 24 genes) Endocrine Disorders - Hyper(Hypo)parathyroidism (24 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Neuropathy (gene panel) Neuropathy panel - UGent Centrum Medische Genetica - UZ Gent
BAP1-related tumor predisposition syndrome (TPDS) BAP1 Familial melanoma Centrum Menselijke Erfelijkheid - KUL
« Inherited bone marrow failures syndromes » with or without organ dysfunction Hematologic Familiar Forms - ULG Centre de Génétique Humaine - CHU Sart-Tilman
Immunodysregulation - polyendocrinopathy - enteropathy - X-linked (IPEX) syndrome FOXP3 Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome Centrum Menselijke Erfelijkheid - KUL
Telomeropathies (virtual gene panel) Centre de Génétique Médicale UCL
Hereditary cancer panel (gene panel) Hereditary Cancer Solution (35 genes) - UCL Centre de Génétique Médicale UCL
Hereditary Polyposis Panel (11 genes) - ULG APC, MUTYH, BMPR1A, NTHL1, SMAD4, MSH3, POLE, POLD1, PTEN, STK11, GREM1 Hereditary Polyposis Panel (11 genes) - ULG Familial adenomatous polyposis, MUTYH-related attenuated familial adenomatous polyposis, Turcot syndrome with polyposis, Hereditary mixed polyposis syndrome, Generalized juvenile polyposis/juvenile polyposis coli Centre de Génétique Humaine - CHU Sart-Tilman
Hereditary Melanoma Panel (7 genes) CDKN2A, CDK4, POT1, TERT, TERF2IP, BAP1, MITF Hereditary Melanoma Panel (7 genes) - ULG Familial melanoma Centre de Génétique Humaine - CHU Sart-Tilman
Hepatology (gene panel) Hepatology panel - UGent Centrum Medische Genetica - UZ Gent
Respiratory disorders (gene panel): non-CF bronchiectasis; pulmonary hypertension; interstitial lung disease Respiratory Disorders panel (137 genes) - Ugent Centrum Medische Genetica - UZ Gent
Kennedy disease (Spinal and bulbar muscular atrophy, SBMA) - CAG repeat expansion AR Kennedy disease Centrum Menselijke Erfelijkheid - KUL
Developmental disorders: intellectual disability and multiple congenital anomalies (gene panel) Developmental disorders: intellectual disability and multiple congenital anomalies (gene panel) - KUL Centrum Menselijke Erfelijkheid - KUL
Arrhytmogenic cardiopathy Arrhytmogenic cardiopathy - UGent Centrum Medische Genetica - UZ Gent
Dilated cardiomyopathy Dilated cardiomyopathy - UGent Centrum Medische Genetica - UZ Gent
VEXAS-syndrome UBA1 VEXAS syndrome Centrum Medische Genetica - UZ Gent
Supravalvular aortic stenosis ELN Centrum Medische Genetica - UZ Gent
Hirschsprung disease Hirschsprung disease - Ugent Hirschsprung disease Centrum Medische Genetica - UZ Gent
Small cell carcinoma of the ovary SMARCA4 Small cell carcinoma of the ovary Centrum Medische Genetica - UZ Gent
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