Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Hereditary Melanoma Panel (7 genes)	CDKN2A, CDK4, POT1, TERT, TERF2IP, BAP1, MITF	Hereditary Melanoma Panel (7 genes) - ULG	Familial melanoma	Centre de Génétique Humaine - CHU Sart-Tilman
Susceptibility to Cutaneous Malignant Melanoma	CDK4		Familial melanoma	Centre de Génétique Humaine - CHU Sart-Tilman
Melanoma (6 genes)	BAP1, CDK4, CDKN2A, MC1R, MITF, POT1	Melanoma (6 genes) - UCL	Familial melanoma, MITF-related melanoma and renal cell carcinoma predisposition syndrome, Uveal melanoma, Melanoma of soft tissue	Centre de Génétique Médicale UCL
Adrenogenital syndrome	CYP21A2		Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form, Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form	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 (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)
Spinocerebellar ataxia (type 13)	KCNC3		Spinocerebellar ataxia type 13	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)

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