Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Neuropathy, Ataxia, and Retinitis Pigmentosa (NARP) syndrome (hot spot mutation - m.8993T>C/G)	MT-ATP6		NARP syndrome	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Hypokalemic periodic paralysis, type 1 (CACNA1S gene hot spot mutations)	CACNA1S		Hypokalemic periodic paralysis	Centrum Medische Genetica - UZ Brussel VUB
Malignant hypertermia	RYR1, CACNA1S		Malignant hyperthermia of anesthesia	Centrum Medische Genetica - UZ Gent
Paraganglioma-pheochromocytoma (gene panel)	SDHA, SDHB, SDHC, SDHD, SDHAF2, RET, VHL, NF1	Paraganglioma-pheochromocytoma (7 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
Parathyroid tumor (gene panel)	CASR, CDC73, MEN1, RET	Parathyroid tumor (4 genes) - KUL	Neonatal severe primary hyperparathyroidism, Familial hypocalciuric hypercalcemia type 1, Autosomal dominant hypocalcemia	Centrum Menselijke Erfelijkheid - KUL

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