Genetic tests

2050100

Search

Full name	Analytes	Gene panels	Disease	Laboratory
Arteriovenous malformation (gene panel)		Arteriovenous malformation (7 genes), Vascular malformations (germline) (38 genes) - UCL	Hereditary hemorrhagic telangiectasia, Heritable pulmonary arterial hypertension, Familial cerebral saccular aneurysm, Vein of Galen aneurysmal malformation, Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome, Capillary malformation-arteriovenous malformation, Parkes Weber syndrome, Microcephaly-capillary malformation syndrome	Centre de Génétique Médicale UCL
Cardiomyopathy, hereditary (gene panel)		Cardiomyopathy, hereditary (208 genes) - VUB	Familial isolated arrhythmogenic ventricular dysplasia, biventricular form, Familial isolated arrhythmogenic ventricular dysplasia, left dominant form, Familial isolated arrhythmogenic ventricular dysplasia, right dominant form, Familial isolated dilated cardiomyopathy, Familial isolated restrictive cardiomyopathy, Left ventricular noncompaction	Centrum Medische Genetica - UZ Brussel VUB
Pulmonary Fibrosis (gene panel) + rs35705950 of MUC5B gene		Pulmonary Fibrosis (21 genes) + rs35705950 (MUC5B gene) - KUL	Idiopathic pulmonary fibrosis	Centrum Menselijke Erfelijkheid - KUL
Cystic Fibrosis / Congenital absence of the vas deferens / CFTR-related disorders (50 hot spot mutations)	CFTR		Cystic fibrosis, Congenital bilateral absence of vas deferens, Idiopathic pulmonary fibrosis, Hereditary chronic pancreatitis	Centrum Medische Genetica - UZ Antwerpen