Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Temple syndrome / Kagami-Ogata Syndrome	DLK1, MEG3, RTL1		Temple syndrome due to maternal uniparental disomy of chromosome 14, Temple syndrome due to paternal 14q32.2 hypomethylation, Temple syndrome due to paternal 14q32.2 microdeletion, Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14, Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation, Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion	Centre de Génétique Médicale UCL
Central Precocious Puberty (5 genes)	MKRN3, KISS1, KISS1R, PROKR2, DLK1	Central Precocious Puberty (5 genes) - ULG	Idiopathic central precocious puberty	Centre de Génétique Humaine - CHU Sart-Tilman
Stickler syndrome (gene panel)	COL2A1, COL11A1, COL9A1, COL9A2	Stickler syndrome (4 genes) - UZA	Stickler syndrome type 1, Stickler syndrome type 2, Autosomal recessive Stickler syndrome	Centrum Medische Genetica - UZ Antwerpen
Renal carcinoma (4 genes)	MET, FH, FLCN, VHL	Renal carcinoma (4 genes) - UCL	Clear cell renal carcinoma	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

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