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
Hyperparathyroidism (gene panel)	AIP, MEN1, CDKN1B, PRKAR1A, RET		Familial isolated hyperparathyroidism	Centre de Génétique Humaine - CHU Sart-Tilman
Multiple endocrine neoplasia type 1 and 4 (MEN1; CDKN1B genes)	MEN1, CDKN1B		Multiple endocrine neoplasia type 1, Multiple endocrine neoplasia type 4	Centrum Menselijke Erfelijkheid - KUL
Multiple endocrine neoplasia, type 1 and 4	MEN1, CDKN1B, AIP		Multiple endocrine neoplasia type 1, Multiple endocrine neoplasia type 4	Centrum Medische Genetica - UZ Gent
Pituitary adenoma (4 genes)	MEN1, AIP, CDKN1B, PRKAR1A	Pituitary adenoma (4 genes) - ULG	Familial isolated pituitary adenoma, Silent pituitary adenoma, Null pituitary adenoma, Multiple endocrine neoplasia type 1, Multiple endocrine neoplasia type 4, Carney complex	Centre de Génétique Humaine - CHU Sart-Tilman
Pituitary adenoma (5 genes)	AIP, CDKN1B, MEN1, RET, PRKAR1A	Pituitary adenoma (5 genes) - UCL	Familial isolated pituitary adenoma, Silent pituitary adenoma, Null pituitary adenoma, Prolactinoma, Pituitary gigantism, Acromegaly	Centre de Génétique Médicale UCL
Multiple endocrine neoplasia (3 genes)	CDKN1B, MEN1, RET	Multiple endocrine neoplasia (3 genes) - UCL	Multiple endocrine neoplasia type 1, Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia type 4	Centre de Génétique Médicale UCL
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
Porencephaly / Hemorrhagic stroke / Cerebral small vessel disease / Idiopathic cerebral white matter lesions / HANAC / Isolated retinal arteriolar tortuosity	COL4A1, COL4A2		Familial porencephaly, HANAC syndrome, Retinal arterial tortuosity	Centrum Medische Genetica - UZ Gent

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