Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Combined immunodeficiency (severe), X-linked	IL2RG		T-B+ severe combined immunodeficiency due to gamma chain deficiency	Centrum Menselijke Erfelijkheid - KUL
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)
Charcot-Marie-Tooth (CMT1A, GJB1)	GJB1, PMP22		X-linked Charcot-Marie-Tooth disease type 1, Charcot-Marie-Tooth disease type 1A	Centre de Génétique Humaine - Erasme ULB
MODY : Maturity onset Diabete of the Young (gene panel)	ABCC8, GCK, HNF1A, HNF4A, HNF1B, INS, KCNJ11	MODY - Maturity onset Diabete of the Young (21 genes) - IPG	MODY	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Hereditary angioneurotic edema (2 genes)	F12, SERPING1		C1 inhibitor deficiency, Hereditary angioedema type 1, Hereditary angioedema type 2	Centre de Génétique Médicale UCL
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)

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