Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Microphthalmia, syndromic 5; Retinal dystrophy, early-onset, and pituitary dysfunction	OTX2		Syndromic microphthalmia type 5, Combined pituitary hormone deficiencies, genetic forms, Butterfly-shaped pigment dystrophy	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
Lipodystrophy (2 genes)	AGPAT2, BSCL2	Lipodystrophy (2 genes) - IPG	Congenital generalized lipodystrophy, Severe neurodegenerative syndrome with lipodystrophy	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Congenital generalized lipodystrophy type 1	AGPAT2		Congenital generalized lipodystrophy	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)

Did not find what you were looking for? Contact us through the support center.