Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)	AIRE		Autoimmune polyendocrinopathy type 1	Centrum Menselijke Erfelijkheid - KUL
Test Biochemical Genetics (Diagnosis of aminoacidopathy, organic aciduria and beta-oxydation defects (amino acids and acylcarnitines by MSMS))	SLC25A20		Carnitine-acylcarnitine translocase deficiency	Sciensano
Hypercholesterolemia (9 genes)	LDLR, APOB, PCSK9, ABCG5, ABCG8, APOE, LDLRAP1, LIPA, STAP1	Hypercholesterolemia (9 genes) - UCL	Homozygous familial hypercholesterolemia	Centre de Génétique Médicale UCL
Hypercholesterolemia, Familial (Gene Panel)	LDLR, APOB, APOE, PCSK9, LDLRAP1	Familial Hypercholesterolemia (9 genes) - IPG	Homozygous familial hypercholesterolemia	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Hypercholesterolemia, Familial (9 genes)	LDLR, APOB, APOE, PCSK9, ABCG5, ABCG8, LDLRAP1, LIPA, STAP1	Familial Hypercholesterolemia panel (9 genes) - ULG	Homozygous familial hypercholesterolemia, Heterozygous familial hypercholesterolemia (NON RARE IN EUROPE), Sitosterolemia, Cholesteryl ester storage disease	Centre de Génétique Humaine - CHU Sart-Tilman
Hypercholesterolemia, Familial (4 genes)	LDLR, APOB, APOE, PCSK9	Familial Hypercholesterolemia panel (4 genes) - KUL	Homozygous familial hypercholesterolemia	Centrum Menselijke Erfelijkheid - KUL
Immune deficiency, X-linked, with hyperIgM	CD40LG		X-linked hyper-IgM syndrome	Centrum Menselijke Erfelijkheid - KUL

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