Genetic tests | Belgian Genetic Tests database

Statistics

Type	Total	Last update
Genetic tests	859	2024-02-16
Diseases	4232	2023-06-22
Analytes	6169	2023-12-20
Gene panels	380	2024-03-20

Full name	Analytes	Gene panels	Disease	Laboratory
Steinert myotonic dystrophy - CTG repeat expansion	DMPK		Steinert myotonic dystrophy	Centrum Menselijke Erfelijkheid - KUL
Steinert myotonic dystrophy - CTG repeat expansion	DMPK		Steinert myotonic dystrophy	Centrum Medische Genetica - UZ Gent
Steinert myotonic dystrophy - CTG repeat expansion	DMPK		Steinert myotonic dystrophy	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Steinert myotonic dystrophy - CTG repeat expansion	DMPK		Steinert myotonic dystrophy	Centrum Medische Genetica - UZ Antwerpen
Steinert myotonic dystrophy - DMPK gene CTG repeat expansion	DMPK		Steinert myotonic dystrophy	Centrum Medische Genetica - UZ Brussel VUB
Steinert myotonic dystrophy - CTG repeat expansion	DMPK		Steinert myotonic dystrophy	Centre de Génétique Humaine - CHU Sart-Tilman
WAGR Syndrome	WT1		WAGR syndrome	Centrum Menselijke Erfelijkheid - KUL
Wilms tumor (DICER1; WT1 genes)	WT1, DICER1	Wilms' tumor (2 genes) - KUL		Centrum Menselijke Erfelijkheid - KUL
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

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