Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Achromatopsia	CNGB3, CNGA3	Achromatopsia (2 genes) - UGent	Achromatopsia	Centrum Medische Genetica - UZ Gent
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 type III (F12 gene - hot spot mutations - p.Thr328Lys; p. Thr328Arg)	F12		F12-related hereditary angioedema with normal C1Inh	Centre de Génétique Humaine - CHU Sart-Tilman
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)
Familial Exudative Vitreoretinopathy, autosomal dominant	FZD4, TSPAN12, LRP5, NDP	Exudative Vitreoretinopathy - UGent	Familial exudative vitreoretinopathy	Centrum Medische Genetica - UZ Gent
Obesity (gene panel)	ADCY3, BDNF, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, SIM1, UCP3	Obesitas (genepanel) - UZA		Centrum Medische Genetica - UZ Antwerpen
Obesitas, early onset (gene panel)	MC4R, MC3R, LEP, LEPR, PCSK1, POMC, SIM1, NTRK2	Obesitas, early onset (8 genes) - VUB		Centrum Medische Genetica - UZ Brussel VUB
Obesitas, Monogenic early onset	MC4R		Obesity due to melanocortin 4 receptor deficiency	Centre de Génétique Humaine - CHU Sart-Tilman

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