Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Fukuyama congenital muscular dystrophy	FKTN		Congenital muscular dystrophy, Fukuyama type	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Hyperparathyroidism (gene panel)	AIP, MEN1, CDKN1B, PRKAR1A, RET		Familial isolated hyperparathyroidism	Centre de Génétique Humaine - CHU Sart-Tilman
Pituitary adenoma (4 genes)	MEN1, AIP, CDKN1B, PRKAR1A	Pituitary adenoma (4 genes) - ULG	Familial isolated pituitary adenoma, Silent pituitary adenoma, Null pituitary adenoma, Multiple endocrine neoplasia type 1, Multiple endocrine neoplasia type 4, Carney complex	Centre de Génétique Humaine - CHU Sart-Tilman
Pituitary adenoma (5 genes)	AIP, CDKN1B, MEN1, RET, PRKAR1A	Pituitary adenoma (5 genes) - UCL	Familial isolated pituitary adenoma, Silent pituitary adenoma, Null pituitary adenoma, Prolactinoma, Pituitary gigantism, Acromegaly	Centre de Génétique Médicale UCL
Carney syndrome	PRKAR1A		Carney complex	Centre de Génétique Médicale UCL
Multiple osteochondromas (2 genes)	EXT1, EXT2	Multiple osteochondromas (2 genes) - UZA	Multiple osteochondromas	Centrum Medische Genetica - UZ Antwerpen
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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