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
Craniosynostosis syndromes (Apert, Crouzon)	FGFR2		Crouzon syndrome, Apert syndrome	Centrum Medische Genetica - UZ Antwerpen
Craniosynostosis / Apert syndrome (hot spot mutations - exon 7)	FGFR2		Apert syndrome	Centre de Génétique Humaine - CHU Sart-Tilman
Hearing loss, STRC gene	STRC		Rare autosomal recessive non-syndromic sensorineural deafness type DFNB	Centrum Medische Genetica - UZ Antwerpen
Recessive nonsyndromic hearing loss and deafness DFNB (2 genes)	GJB2, GJB6		Rare autosomal recessive non-syndromic sensorineural deafness type DFNB	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Deafness, autosomal recessive 1A	GJB2		Rare autosomal recessive non-syndromic sensorineural deafness type DFNB	Centrum Medische Genetica - UZ Antwerpen
Frequent hearing deficiency (4 genes)	GJB2, GJB6, STRC, OTOA		Rare autosomal recessive non-syndromic sensorineural deafness type DFNB	Centre de Génétique Humaine - Erasme ULB
Recessive nonsyndromic hearing loss and deafness (2 genes)	GJB2, GJB6	Non syndromic hearing loss and deafness (2 genes) - IPG - ULG	Rare autosomal recessive non-syndromic sensorineural deafness type DFNB	Centre de Génétique Humaine - CHU Sart-Tilman
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
Becker muscular dystrophy / Duchenne muscular dystrophy (deletion/duplication DMD gene)	DMD		Duchenne muscular dystrophy, Becker muscular dystrophy, Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers	Centrum Menselijke Erfelijkheid - KUL
Becker muscular dystrophy / Duchenne muscular dystrophy (deletion/duplication DMD gene)	DMD		Duchenne muscular dystrophy, Becker muscular dystrophy, Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Becker muscular dystrophy / Duchenne muscular dystrophy (deletion/duplication DMD gene)	DMD		Duchenne muscular dystrophy, Becker muscular dystrophy, Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers	Centrum Medische Genetica - UZ Antwerpen
Becker muscular dystrophy / Duchenne muscular dystrophy (Full sequencing DMD gene through Myopathy gene panel)	DMD		Duchenne muscular dystrophy, Becker muscular dystrophy, Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers	Centrum Medische Genetica - UZ Antwerpen
Becker muscular dystrophy / Duchenne muscular dystrophy (deletion/duplication DMD gene)	DMD		Duchenne muscular dystrophy, Becker muscular dystrophy, Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers	Centre de Génétique Humaine - CHU Sart-Tilman

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