Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Nijmegen Breakage Syndrome	NBN		Nijmegen breakage syndrome	Centrum Menselijke Erfelijkheid - KUL
Nijmegen breakage syndrome	NBN		Nijmegen breakage syndrome	Centrum Medische Genetica - UZ Gent
Hereditary cancer (Breast, ovary, colon) (26 genes)	BRCA1, BRCA2, BARD1, BRIP1, CDH1, MLH1, MSH2, MSH6, MEN1, PTEN, RAD50, RAD51D, STK11, TP53, CHEK2, MUTYH, PALB2, RAD51C, ATM, EPCAM, BLM, NBN, PMS2, XRCC2, ABRAXAS1, MRE11	Cancer (Breast, ovary, colon,…) (26 genes) - ULG		Centre de Génétique Humaine - CHU Sart-Tilman
Long chain 3-hydroxyl-CoA dehydrogenase deficiency (hot spot mutation - p.Glu510Gln)	HADHA		Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
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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