Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
MODY : Maturity onset Diabete of the Young (gene panel)	ABCC8, GCK, HNF1A, HNF4A, HNF1B, INS, KCNJ11	MODY - Maturity onset Diabete of the Young (21 genes) - IPG	MODY	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Polyarteritis nodosa, childhood-onset / Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome	ADA2		Vasculitis due to ADA2 deficiency, Diamond-Blackfan anemia, Sneddon syndrome	Centrum Menselijke Erfelijkheid - KUL
Resistance to vitamin K antagonists - VKORC1 sequencing (all exons ) - Pharmacogenetics	VKORC1		Resistance to vitamin K antagonists, Prediction of resistance to vitamin K antagonists	Centre de Génétique Médicale UCL
Vitamin K antagonists toxicity or dose selection - VKORC1 genotyping (-1639G>A + 1173C>T) - Pharmacogenetics	VKORC1		Vitamin K antagonists toxicity or dose selection, Prediction of toxicity or dose selection of vitamin K antagonists	Centre de Génétique Médicale UCL
Deficiency of Vitamin K-Dependent Clotting Factors	VKORC1, GGCX		Hereditary combined deficiency of vitamin K-dependent clotting factors	Centrum Medische Genetica - UZ Gent
Silver-Russell syndrome	11p15.5, 7p12.1, 7q32.2		Silver-Russell syndrome, Silver-Russell syndrome due to an imprinting defect of 11p15, Silver-Russell syndrome due to 11p15 microduplication	Centre de Génétique Médicale UCL
Uniparental disomy	7p12.1, 7q32.2		Silver-Russell syndrome	Centre de Génétique Médicale UCL

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