Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Gorlin syndrome (gene panel)	PTCH1, PTCH2, SUFU	Gorlin syndrome (3 genes)	Gorlin syndrome	Centre de Génétique Médicale UCL
Medulloblastoma (gene panel)	SUFU, TP53, PTCH1	Medulloblastoma (3 genes) - KUL	Medulloblastoma	Centrum Menselijke Erfelijkheid - KUL
Medulloblastoma (3 genes)	PTCH1, PTCH2, SUFU	Medulloblastoma (3 genes) - UCL	Medulloblastoma , Gorlin syndrome	Centre de Génétique Médicale UCL
Feingold syndrome	MYCN		Feingold syndrome type 1	Centrum Medische Genetica - UZ Gent
Hereditary cancer (Breast, ovary, colon) (26 genes)	BRCA1, BRCA2, BARD1, BRIP1, CDH1, MLH1, MSH2, MSH6, MEN1, PTEN, RAD50, RAD51D, STK11, TP53, CHEK2, MUTYH, PALB2, RAD51C, ATM, EPCAM, BLM, NBN, PMS2, XRCC2, ABRAXAS1, MRE11	Cancer (Breast, ovary, colon,…) (26 genes) - ULG		Centre de Génétique Humaine - CHU Sart-Tilman
Congenital hemangioma (2 genes)	GNAQ, GNA11		Familial multiple nevi flammei, Sturge-Weber syndrome, Uveal melanoma	Centrum Menselijke Erfelijkheid - KUL
Hypocalciuric hypercalcemia, familial type II	GNA11		Familial hypocalciuric hypercalcemia type 2	Centre de Génétique Humaine - CHU Sart-Tilman
Vascular malformations (somatic)	AKT1, AKT2, AKT3, ALK, BRAF, GNA11, GNA14, GNAQ, HRAS, IDH1, IDH2, KRAS, NRAS, PIK3CA, PIK3R1, PIK3R2, PTEN, TEK, MAP3K3, MAP2K1	Vascular malformations (somatic) (19 genes) - UCL	Capillary malformation-arteriovenous malformation, CLOVES syndrome, Maffucci syndrome, Proteus syndrome	Centre de Génétique Médicale UCL

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