Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Tuberous sclerosis	TSC1, TSC2		Tuberous sclerosis complex	Centrum Medische Genetica - UZ Gent
Tuberous sclerosis (2 genes)	TSC1, TSC2		Tuberous sclerosis complex	Centre de Génétique Médicale UCL
Immunodeficiency 30 / Susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency	IL12RB1		Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency	Centrum Menselijke Erfelijkheid - KUL
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)
Congenital hemangioma (2 genes)	GNAQ, GNA11		Familial multiple nevi flammei, Sturge-Weber syndrome, Uveal melanoma	Centrum Menselijke Erfelijkheid - KUL
Hypocalciuric hypercalcemia, familial type II	GNA11		Familial hypocalciuric hypercalcemia type 2	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

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