Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Familial Exudative Vitreoretinopathy, autosomal dominant	FZD4, TSPAN12, LRP5, NDP	Exudative Vitreoretinopathy - UGent	Familial exudative vitreoretinopathy	Centrum Medische Genetica - UZ Gent
Norrie disease (NDP gene)	NDP		Norrie disease	Centrum Medische Genetica - UZ Brussel VUB
Overgrowth & vascular anomalies / CLOVES syndrome	PIK3CA		CLOVES syndrome	Centrum Menselijke Erfelijkheid - KUL
Vascular malformations (somatic)	AKT1, AKT2, AKT3, ALK, BRAF, GNA11, GNA14, GNAQ, HRAS, IDH1, IDH2, KRAS, NRAS, PIK3CA, PIK3R1, PIK3R2, PTEN, TEK, MAP3K3, MAP2K1	Vascular malformations (somatic) (19 genes) - UCL	Capillary malformation-arteriovenous malformation, CLOVES syndrome, Maffucci syndrome, Proteus syndrome	Centre de Génétique Médicale UCL
Bronchiectasis (4 genes)	CFTR, SCNN1A, SCNN1B, SCNN1G	Bronchiectasis (4 genes) - UCL	Idiopathic bronchiectasis	Centre de Génétique Médicale UCL
Bronchiectasies with or without elevated sweat chloride panel (5 genes)	CFTR, SCNN1A, SCNN1B, SCNN1G	Pulmonary/Bronchiectasies (5 genes) - IPG	Idiopathic bronchiectasis, Cystic fibrosis	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Hereditary Angioedema (7 genes)	PLG, F12, SERPING1, ANGPT1, KNG1	Angioedema (7 genes) - IPG	F12-related hereditary angioedema with normal C1Inh, Hereditary angioedema type 1, Hereditary angioedema type 2, PLG-related hereditary angioedema with normal C1Inh	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)

Did not find what you were looking for? Contact us through the support center.