Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Autoimmune disease, multisystem, infantile-onset (ADMIO) / Hyper-IgE recurrent infection syndrome	STAT3		STAT3-related early-onset multisystem autoimmune disease, Autosomal dominant hyper-IgE syndrome	Centrum Menselijke Erfelijkheid - KUL
BAP1-tumor predisposition syndrome	BAP1		BAP1-related tumor predisposition syndrome	Centrum Medische Genetica - UZ Gent
BAP1-related tumor predisposition syndrome (TPDS)	BAP1		Familial melanoma	Centrum Menselijke Erfelijkheid - KUL
Hereditary Melanoma Panel (7 genes)	CDKN2A, CDK4, POT1, TERT, TERF2IP, BAP1, MITF	Hereditary Melanoma Panel (7 genes) - ULG	Familial melanoma	Centre de Génétique Humaine - CHU Sart-Tilman
Malignant Mesothelioma (BAP1; CDKN2A genes)	BAP1, CDKN2A			Centrum Menselijke Erfelijkheid - KUL
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
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

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