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
Leiomyomatosis and renal cell cancer	FH		Hereditary leiomyomatosis and renal cell cancer	Centre de Génétique Médicale UCL
Renal carcinoma (4 genes)	MET, FH, FLCN, VHL	Renal carcinoma (4 genes) - UCL	Clear cell renal carcinoma	Centre de Génétique Médicale UCL
Hemochromatosis hereditary type 2 to type 5 (5 genes)	HAMP, FTH1, SLC40A1, TFR2, HJV	Hemochromatosis hereditary (types 2 to 5) (5 genes) - UCL	HJV or HAMP-related hemochromatosis, TFR2-related hemochromatosis, Hemochromatosis type 4, Hemochromatosis type 5	Centre de Génétique Médicale UCL
Hemochromatosis, juvenile (HJV and HAMP genes)	HAMP		HJV or HAMP-related hemochromatosis	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
Frequent hearing deficiency (4 genes)	GJB2, GJB6, STRC, OTOA		Rare autosomal recessive non-syndromic sensorineural deafness type DFNB	Centre de Génétique Humaine - Erasme ULB

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