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
Pompe disease, Glycogen storage disease II (GAA gene)	GAA		Glycogen storage disease due to acid maltase deficiency, infantile onset, Glycogen storage disease due to acid maltase deficiency, late-onset	Centrum Medische Genetica - UZ Brussel VUB
Spinocerebellar ataxia (types 1, 2, 3, 6, 7) - CAG repeat expansion	ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7	Spinocerebellar ataxia (types 1, 2, 3, 6, 7) (5 genes) - KUL	Spinocerebellar ataxia type 1, Spinocerebellar ataxia type 2, Machado-Joseph disease type 3, Spinocerebellar ataxia type 6, Spinocerebellar ataxia type 7	Centrum Menselijke Erfelijkheid - KUL
Spinocerebellar ataxia (types 1, 2, 3, 6, 7, 17) - CAG repeat expansion	ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, TBP	Spinocerebellar ataxia (types 1, 2, 3, 6, 7, 17) (6 genes) - IPG	Spinocerebellar ataxia type 1, Spinocerebellar ataxia type 2, Machado-Joseph disease type 3, Spinocerebellar ataxia type 6, Spinocerebellar ataxia type 7, Spinocerebellar ataxia type 17	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Spinocerebellar ataxia (SCA) types 1, 2, 3, 6, 7 - CAG repeat expansion	ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7	Spinocerebellar ataxia (types 1, 2, 3, 6, 7) (5 genes) - UZA	Spinocerebellar ataxia type 1, Spinocerebellar ataxia type 2, Machado-Joseph disease type 3, Spinocerebellar ataxia type 6, Spinocerebellar ataxia type 7	Centrum Medische Genetica - UZ Antwerpen
Spinocerebellar ataxia (types 1, 2, 3, 6, 7) - CAG repeat expansion	ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7	Spinocerebellar ataxia (types 1, 2, 3, 6, 7) (5 genes) - VUB	Spinocerebellar ataxia type 1, Spinocerebellar ataxia type 2, Machado-Joseph disease type 3, Spinocerebellar ataxia type 6, Spinocerebellar ataxia type 7	Centrum Medische Genetica - UZ Brussel VUB
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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