Genetic tests

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Full name	Analytes	Gene panels	Disease	Laboratory
Hemophilia A	F8		Hemophilia A, Severe hemophilia A, Moderate hemophilia A, Mild hemophilia A, Bleeding disorder in hemophilia A carriers	Centre de Génétique Médicale UCL
Hemophilia A (inversions)	F8		Severe hemophilia A, Bleeding disorder in hemophilia A carriers	Centre de Génétique Médicale UCL
Hemophilia A	F8		Hemophilia A, Mild hemophilia A, Severe hemophilia A, Moderate hemophilia A, Bleeding disorder in hemophilia A carriers	Centrum Menselijke Erfelijkheid - KUL
Polycystic kidney disease type 1 and 2	PKD1, PKD2		Autosomal dominant polycystic kidney disease, Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis	Centrum Medische Genetica - UZ Gent
Sessile serrated polyposis syndrome (RNF43 gene)	RNF43		Serrated polyposis syndrome	Centre de Génétique Humaine - CHU Sart-Tilman
Medium chain acyl-CoA dehydrogenase deficiency (MCAD hot spot mutation - p.Lys329Glu)	ACADM		Medium chain acyl-CoA dehydrogenase deficiency	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Medium chain acyl-CoA dehydrogenase deficiency (MCAD-ACADM)	ACADM		Medium chain acyl-CoA dehydrogenase deficiency	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Medium chain acyl-CoA dehydrogenase deficiency (MCAD-ACADM gene)	ACADM		Medium chain acyl-CoA dehydrogenase deficiency	Centrum Medische Genetica - UZ Brussel VUB
Medium chain acyl-CoA dehydrogenase deficiency (MCAD hot spot mutation - p.Lys329Glu)	ACADM		Medium chain acyl-CoA dehydrogenase deficiency	Centre de Génétique Humaine - CHU Sart-Tilman