Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Bloom syndrome	BLM		Bloom syndrome	Centrum Medische Genetica - UZ Gent
Bloom syndrome	BLM		Bloom syndrome	Centrum Menselijke Erfelijkheid - KUL
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
Cardiofaciocutaneous syndrome (5 genes)	HRAS, KRAS, BRAF, MAP2K2, MAP2K1		Cardiofaciocutaneous syndrome	Centre de Génétique Humaine - CHU Sart-Tilman
Costello Syndrome- Schimmelpenning syndrome	HRAS		Costello syndrome	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
Agnathia-otocephaly complex	PRRX1		Agnathia-holoprosencephaly-situs inversus syndrome	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Blepharophimosis type I /II	FOXL2		Blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome, Blepharophimosis-epicanthus inversus-ptosis due to copy number variations	Centrum Medische Genetica - UZ Gent

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