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
Hallervorden-Spatz disease (Neurodegeneration with brain iron accumulation type 1) / HARP syndrome (Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis pigmentosa, and Pallidal degeneration)	PANK2		Classic pantothenate kinase-associated neurodegeneration, Atypical pantothenate kinase-associated neurodegeneration	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Lissencephaly / subcortical band heterotopia	PAFAH1B1		Lissencephaly due to LIS1 mutation, Subcortical band heterotopia	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Lissencephaly (LIS1 gene)	PAFAH1B1		Lissencephaly due to LIS1 mutation	Centrum Medische Genetica - UZ Brussel VUB
Porencephaly / Hemorrhagic stroke / Cerebral small vessel disease / Idiopathic cerebral white matter lesions / HANAC / Isolated retinal arteriolar tortuosity	COL4A1, COL4A2		Familial porencephaly, HANAC syndrome, Retinal arterial tortuosity	Centrum Medische Genetica - UZ Gent

Did not find what you were looking for? Contact us through the support center.