Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Hereditary angioneurotic edema (2 genes)	F12, SERPING1		C1 inhibitor deficiency, Hereditary angioedema type 1, Hereditary angioedema type 2	Centre de Génétique Médicale UCL
Hereditary angioedema type III (F12 gene - hot spot mutations - p.Thr328Lys; p. Thr328Arg)	F12		F12-related hereditary angioedema with normal C1Inh	Centre de Génétique Humaine - CHU Sart-Tilman
Hereditary Angioedema (7 genes)	PLG, F12, SERPING1, ANGPT1, KNG1	Angioedema (7 genes) - IPG	F12-related hereditary angioedema with normal C1Inh, Hereditary angioedema type 1, Hereditary angioedema type 2, PLG-related hereditary angioedema with normal C1Inh	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Rhabdomyosarcoma	DICER1, NF1, TP53			Centrum Menselijke Erfelijkheid - KUL
Neurofibromatosis type 1 / Legius syndrome (2 genes)	NF1, SPRED1		Neurofibromatosis type 1, Legius syndrome	Centrum Menselijke Erfelijkheid - KUL
Paraganglioma-pheochromocytoma (gene panel)	SDHA, SDHB, SDHC, SDHD, SDHAF2, RET, VHL, NF1	Paraganglioma-pheochromocytoma (7 genes) - KUL	Hereditary pheochromocytoma-paraganglioma	Centrum Menselijke Erfelijkheid - KUL
Neurofibromatosis type I	NF1		Neurofibromatosis type 1	Centre de Génétique Médicale UCL
Neurofibromatosis type 1 / Legius syndrome	NF1, SPRED1		Neurofibromatosis type 1, Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion, 17q11 microdeletion syndrome, Legius syndrome	Centrum Medische Genetica - UZ Gent

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