Genetic tests

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Full name	Analytes	Gene panels	Disease	Laboratory
Neurofibromatosis type 1 / Legius syndrome (2 genes)	NF1, SPRED1		Neurofibromatosis type 1, Legius syndrome	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
Paraganglioma-pheochromocytoma (gene panel)		Paraganglioma-pheochromocytoma (8 genes) - KUL	Hereditary pheochromocytoma-paraganglioma	Centrum Menselijke Erfelijkheid - KUL
Pheochromocytoma - paraganglioma syndrome (gene panel)	SDHB, SDHC, SDHD, SDHA, MAX, TMEM127, SDHAF2, VHL, RET, SUCLG2	Pheochromocytoma - paraganglioma syndrome - UGent	Hereditary pheochromocytoma-paraganglioma	Centrum Medische Genetica - UZ Gent
Paraganglioma-pheochromocytoma (6 genes) - ULG	RET, VHL, SDHA, SDHB, SDHC, SDHD	Paraganglioma-pheochromocytoma (6 genes) - ULG	Hereditary pheochromocytoma-paraganglioma, Von Hippel-Lindau disease, Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia type 2A	Centre de Génétique Humaine - CHU Sart-Tilman
Melanoma (6 genes)	BAP1, CDK4, CDKN2A, MC1R, MITF, POT1	Melanoma (6 genes) - UCL	Familial melanoma, MITF-related melanoma and renal cell carcinoma predisposition syndrome, Uveal melanoma, Melanoma of soft tissue	Centre de Génétique Médicale UCL