Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
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
Bronchiectasis (4 genes)	CFTR, SCNN1A, SCNN1B, SCNN1G	Bronchiectasis (4 genes) - UCL	Idiopathic bronchiectasis	Centre de Génétique Médicale UCL
Bronchiectasies with or without elevated sweat chloride panel (5 genes)	CFTR, SCNN1A, SCNN1B, SCNN1G	Pulmonary/Bronchiectasies (5 genes) - IPG	Idiopathic bronchiectasis, Cystic fibrosis	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
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
Mental retardation, X-linked, syndromic, Borck type	EIF2S3		MEHMO syndrome	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)

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