Genetic tests

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Full name	Analytes	Gene panels	Disease	Laboratory
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
Cylindromatosis	CYLD		Familial cylindromatosis	Centre de Génétique Médicale UCL
Thanatophoric dysplasia (hot spot mutations - p.Arg248 / p.Gly370 / p.Ser371 / p.Tyr373 / p.Lys650 / p.X806 in FGFR3 gene)	FGFR3		Thanatophoric dysplasia type 2, Thanatophoric dysplasia type 1	Centrum Medische Genetica - UZ Gent
Thanatophoric dysplasia types 1 and 2 (hot spot mutation - p.Lys650Glu)	FGFR3		Thanatophoric dysplasia type 1, Thanatophoric dysplasia type 2	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Thanatophoric dysplasia (hot spot mutations - p.Tyr373Cys, p.Arg248Cys, p.Ser249Cys)	FGFR3		Thanatophoric dysplasia type 1, Thanatophoric dysplasia type 2	Centrum Medische Genetica - UZ Antwerpen