Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Disease	Laboratory
Friedreich ataxia - GAA repeat expansion	FXN	Friedreich ataxia	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Friedreich ataxia - GAA repeat expansion	FXN	Friedreich ataxia	Centre de Génétique Humaine - CHU Sart-Tilman
Friedreich ataxia - GAA repeat expansion	FXN	Friedreich ataxia	Centrum Menselijke Erfelijkheid - KUL
Microphthalmia, syndromic 5; Retinal dystrophy, early-onset, and pituitary dysfunction	OTX2	Syndromic microphthalmia type 5, Combined pituitary hormone deficiencies, genetic forms, Butterfly-shaped pigment dystrophy	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Neurofibromatosis type 1 / Legius syndrome (2 genes)	NF1, SPRED1	Neurofibromatosis type 1, Legius syndrome	Centrum Menselijke Erfelijkheid - KUL
Neurofibromatosis type 1 / Legius syndrome	NF1, SPRED1	Neurofibromatosis type 1, Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion, 17q11 microdeletion syndrome, Legius syndrome	Centrum Medische Genetica - UZ Gent
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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