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
Breast and Ovarian Cancer, HBOC, Familial (17 genes)	BRCA1, BRCA2, TP53, PALB2, CHEK2, ATM, BRIP1, RAD51C, RAD51D, MLH1, MSH2, MSH6, BARD1, CDH1, EPCAM, PMS2, PTEN		Hereditary breast and/or ovarian cancer syndrome	Centre de Génétique Médicale UCL
Breast and Ovarian Cancer, HBOC, Hereditary		Breast and ovarian cancer - UGent	Hereditary breast cancer, Hereditary breast and/or ovarian cancer syndrome	Centrum Medische Genetica - UZ Gent
Breast cancer, hereditary / Li-Fraumeni syndrome (Hot spot mutation - 1100delC)	CHEK2		Li-Fraumeni syndrome, Hereditary breast and/or ovarian cancer syndrome	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Breast and Ovarian Cancer, hereditary, HBOC, Familial (gene panel)	BRCA1, BRCA2, PALB2, TP53, CHEK2, ATM, BRIP1, RAD51C, RAD51D, MLH1, MSH2, MSH6, BARD1	Breast/ ovarian cancer (12 genes) - UZA	Hereditary breast cancer, Hereditary breast and/or ovarian cancer syndrome	Centrum Medische Genetica - UZ Antwerpen
Hereditary Breast and Ovarian Cancer, HBOC (13 genes)	BRCA1, BRCA2, TP53, PALB2, CHEK2, MLH1, MSH2, MSH6, BRIP1, BARD1, RAD51C, RAD51D, ATM	Breast cancer, hereditary (13 genes) - ULG	Hereditary breast cancer, Hereditary breast and/or ovarian cancer syndrome	Centre de Génétique Humaine - CHU Sart-Tilman
Breast and Ovarian Cancer, HBOC, Familial (12 genes)		Breast/Ovarian cancer (12 genes) - IPG	Hereditary breast and/or ovarian cancer syndrome	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Uniparental Disomy (UDP7; UDP11; UDP14; UDP15; UDP16)			Paternal uniparental disomy of chromosome 7, Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7, Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11, Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11, Temple syndrome due to maternal uniparental disomy of chromosome 14, Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14, Angelman syndrome due to paternal uniparental disomy of chromosome 15, Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15, Maternal uniparental disomy of chromosome 16	Centrum Medische Genetica - UZ Gent
Uniparental Disomy (UDP7; UDP11; UDP14; UDP20)			Paternal uniparental disomy of chromosome 7, Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7, Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11, Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11, Temple syndrome due to maternal uniparental disomy of chromosome 14, Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14	Centrum Menselijke Erfelijkheid - KUL
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

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