Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Hemophilia A	F8		Hemophilia A, Severe hemophilia A, Moderate hemophilia A, Mild hemophilia A, Bleeding disorder in hemophilia A carriers	Centre de Génétique Médicale UCL
Hemophilia A (inversions)	F8		Severe hemophilia A, Bleeding disorder in hemophilia A carriers	Centre de Génétique Médicale UCL
Hemophilia A	F8		Hemophilia A, Mild hemophilia A, Severe hemophilia A, Moderate hemophilia A, Bleeding disorder in hemophilia A carriers	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
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
Currarino syndrome	MNX1		Currarino syndrome	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
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)

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