Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Leber hereditary optic neuropathy (LHON) (hot spot mutations - p.Ala53Thr in MT-ND1; p.Arg340His in MT-ND4; p.Met64Val in MT-ND6)	MT-ND1, MT-ND4, MT-ND6		Leber hereditary optic neuropathy	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Leber hereditary optic neuropathy (LHON) (hot spot mutations - p.Ala53Thr in MT-ND1; p.Arg340His in MT-ND4; p.Met64Val in MT-ND6)	MT-ND1, MT-ND4, MT-ND6	LHON (3 genes) - VUB	Leber hereditary optic neuropathy	Centrum Medische Genetica - UZ Brussel VUB
Lymphoproliferative syndrome, X-linked (XIAP gene)	XIAP		X-linked lymphoproliferative disease, X-linked lymphoproliferative disease due to XIAP deficiency	Centrum Menselijke Erfelijkheid - KUL
Pancreatitis, hereditary (7 genes)	CASR, CFTR, CLDN2, CPA1, CTRC, PRSS1, SPINK1	Pancreatitis (7 genes) - UCL	Hereditary chronic pancreatitis	Centre de Génétique Médicale UCL
Pancreatitis, hereditary (7 genes)	CASR, CFTR, CLDN2, CPA1, CTRC, PRSS1, SPINK1	Pancreatitis (7 genes) - ULB	Hereditary chronic pancreatitis	Centre de Génétique Humaine - Erasme ULB
Pancreatitis, idiopathic or hereditary (7 genes)	CFTR, SPINK1, PRSS1, CTRC, CASR, CLDN2, CPA1	Pancreatitis (7 genes) - ULG		Centre de Génétique Humaine - CHU Sart-Tilman
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

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