Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Waardenburg Syndrome types I and III	PAX3		Waardenburg syndrome type 1, Waardenburg syndrome type 3	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Waardenburg syndrome (gene panel)	EDN3, EDNRB, MITF, PAX3, SNAI2, SOX10	Waardenburg syndrome (6 genes) - UZA	Waardenburg syndrome type 1, Waardenburg syndrome type 2, Waardenburg syndrome type 3, Waardenburg-Shah syndrome	Centrum Medische Genetica - UZ Antwerpen
Hyperthyroidism ( familial gestational or familial nonautoimmune, hypothyroidism, thyrotropin) - TSHR	TSHR		Familial hyperthyroidism due to mutations in TSH receptor, Hypothyroidism due to TSH receptor mutations, Familial gestational hyperthyroidism	Centre de Génétique Humaine - Erasme ULB
BAP1-tumor predisposition syndrome	BAP1		BAP1-related tumor predisposition syndrome	Centrum Medische Genetica - UZ Gent
BAP1-related tumor predisposition syndrome (TPDS)	BAP1		Familial melanoma	Centrum Menselijke Erfelijkheid - KUL
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
Malignant Mesothelioma (BAP1; CDKN2A genes)	BAP1, CDKN2A			Centrum Menselijke Erfelijkheid - KUL
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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