Genetic tests | Belgian Genetic Tests database

Statistics

Type	Total	Last update
Genetic tests	859	2024-02-16
Diseases	4232	2023-06-22
Analytes	6169	2023-12-20
Gene panels	380	2024-03-20

Full name	Analytes	Gene panels	Disease	Laboratory
Von Willebrand disease	VWF		Von Willebrand disease type 1, Von Willebrand disease type 2A, Von Willebrand disease type 2M, Von Willebrand disease type 2B, Von Willebrand disease type 2N, Von Willebrand disease type 3	Centrum Medische Genetica - UZ Antwerpen
Pancreatitis, hereditary (7 genes)	CASR, CFTR, CLDN2, CPA1, CTRC, PRSS1, SPINK1	Pancreatitis (7 genes) - UCL	Hereditary chronic pancreatitis	Centre de Génétique Médicale UCL
Pancreatitis, hereditary (2 genes)	PRSS1, SPINK1		Hereditary chronic pancreatitis	Centrum Medische Genetica - UZ Gent
Pancreatitis, hereditary (7 genes)	CASR, CFTR, CLDN2, CPA1, CTRC, PRSS1, SPINK1	Pancreatitis (7 genes) - ULB	Hereditary chronic pancreatitis	Centre de Génétique Humaine - Erasme ULB
Pancreatitis hereditary (PRSS1 gene)	PRSS1		Hereditary chronic pancreatitis	Centre de Génétique Humaine - CHU Sart-Tilman
Pancreatitis, idiopathic or hereditary (7 genes)	CFTR, SPINK1, PRSS1, CTRC, CASR, CLDN2, CPA1	Pancreatitis (7 genes) - ULG		Centre de Génétique Humaine - CHU Sart-Tilman
Leri-Weill dyschondrosteosis / SHOX-related short stature	SHOX		Léri-Weill dyschondrosteosis, SHOX-related short stature	Centrum Medische Genetica - UZ Gent
Leri-Weill dyschondrosteosis / SHOX-related short stature	SHOX		Léri-Weill dyschondrosteosis, SHOX-related short stature	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Leri-Weill dyschondrosteosis / SHOX-related short stature	SHOX		Léri-Weill dyschondrosteosis, SHOX-related short stature	Centrum Medische Genetica - UZ Antwerpen
Leri-Weill dyschondrosteosis / ISS	SHOX		Léri-Weill dyschondrosteosis, SHOX-related short stature	Centre de Génétique Humaine - CHU Sart-Tilman
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

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