Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Stickler syndrome (gene panel)	COL2A1, COL11A1, COL9A1, COL9A2	Stickler syndrome (4 genes) - UZA	Stickler syndrome type 1, Stickler syndrome type 2, Autosomal recessive Stickler syndrome	Centrum Medische Genetica - UZ Antwerpen
Fanconi anemia (FANCC) (hot spot mutation - c.456+4A>T)	FANCC		Fanconi anemia	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
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)
Non-cholestatic jaundice with direct bilirubin (3 genes)	ABCC2, SLCO1B1, SLCO1B3	Non-cholestatic jaundice with direct bilirubin (3 genes) - UCL	Rotor syndrome, Dubin-Johnson syndrome	Centre de Génétique Médicale UCL

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