Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Aarskog-Scott syndrome	FGD1		Aarskog-Scott syndrome	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
Agnathia-otocephaly complex	PRRX1		Agnathia-holoprosencephaly-situs inversus syndrome	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Hallervorden-Spatz disease (Neurodegeneration with brain iron accumulation type 1) / HARP syndrome (Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis pigmentosa, and Pallidal degeneration)	PANK2		Classic pantothenate kinase-associated neurodegeneration, Atypical pantothenate kinase-associated neurodegeneration	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)

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