Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Dysautonomia, familial (FD) (hot spot mutation - c.2204+6T>C)	ELP1		Familial dysautonomia	Centrum Medische Genetica - UZ Antwerpen
Jewish mutation panel (Tay Sachs, Fanconi, Dysautonomia, Canavan) (4 genes; 7 hot spot mutations)	ASPA, ELP1, HEXA, FANCC	Hot spot mutation among Jewish (4 genes, 7 mutations) - UZA		Centrum Medische Genetica - UZ Antwerpen
Hemochromatosis hereditary type 2 to type 5 (5 genes)	HAMP, FTH1, SLC40A1, TFR2, HJV	Hemochromatosis hereditary (types 2 to 5) (5 genes) - UCL	HJV or HAMP-related hemochromatosis, TFR2-related hemochromatosis, Hemochromatosis type 4, Hemochromatosis type 5	Centre de Génétique Médicale UCL
Hemochromatosis hereditary type 4 (SLC40A1 gene)	SLC40A1		Hemochromatosis type 4	Centre de Génétique Humaine - CHU Sart-Tilman
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)
Familial Exudative Vitreoretinopathy, autosomal dominant	FZD4, TSPAN12, LRP5, NDP	Exudative Vitreoretinopathy - UGent	Familial exudative vitreoretinopathy	Centrum Medische Genetica - UZ Gent

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