Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Gorlin syndrome (gene panel)	PTCH1, PTCH2, SUFU	Gorlin syndrome (3 genes)	Gorlin syndrome	Centre de Génétique Médicale UCL
Medulloblastoma (gene panel)	SUFU, TP53, PTCH1	Medulloblastoma (3 genes) - KUL	Medulloblastoma	Centrum Menselijke Erfelijkheid - KUL
Medulloblastoma (3 genes)	PTCH1, PTCH2, SUFU	Medulloblastoma (3 genes) - UCL	Medulloblastoma , Gorlin syndrome	Centre de Génétique Médicale UCL
Neuroblastoma (2 genes)	ALK, PHOX2B	Neuroblastoma (2 genes) - UCL	Neuroblastoma	Centre de Génétique Médicale UCL
Vascular malformations (somatic)	AKT1, AKT2, AKT3, ALK, BRAF, GNA11, GNA14, GNAQ, HRAS, IDH1, IDH2, KRAS, NRAS, PIK3CA, PIK3R1, PIK3R2, PTEN, TEK, MAP3K3, MAP2K1	Vascular malformations (somatic) (19 genes) - UCL	Capillary malformation-arteriovenous malformation, CLOVES syndrome, Maffucci syndrome, Proteus syndrome	Centre de Génétique Médicale UCL
Autosomal dominant non-syndromic sensorineural deafness type DFNA9 (COCH partial sequencing)	COCH		Rare autosomal dominant non-syndromic sensorineural deafness type DFNA	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Hearing loss (deafness), autosomal dominant 9 (COCH exons 4 and 5)	COCH		Rare autosomal dominant non-syndromic sensorineural deafness type DFNA	Centrum Medische Genetica - UZ Antwerpen
Hyperoxaluria	AGXT, GRHPR, HOGA1		Primary hyperoxaluria type 1, Primary hyperoxaluria type 2, Primary hyperoxaluria type 3	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)

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