Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Leber hereditary optic neuropathy (LHON) (hot spot mutations - p.Ala53Thr in MT-ND1; p.Arg340His in MT-ND4; p.Met64Val in MT-ND6)	MT-ND1, MT-ND4, MT-ND6		Leber hereditary optic neuropathy	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Leber hereditary optic neuropathy (LHON) (hot spot mutations - p.Ala53Thr in MT-ND1; p.Arg340His in MT-ND4; p.Met64Val in MT-ND6)	MT-ND1, MT-ND4, MT-ND6	LHON (3 genes) - VUB	Leber hereditary optic neuropathy	Centrum Medische Genetica - UZ Brussel VUB
Gorlin syndrome (gene panel)	PTCH1, PTCH2, SUFU	Gorlin syndrome (3 genes)	Gorlin syndrome	Centre de Génétique Médicale UCL
Medulloblastoma (gene panel)	SUFU, TP53, PTCH1	Medulloblastoma (3 genes) - KUL	Medulloblastoma	Centrum Menselijke Erfelijkheid - KUL
Medulloblastoma (3 genes)	PTCH1, PTCH2, SUFU	Medulloblastoma (3 genes) - UCL	Medulloblastoma , Gorlin syndrome	Centre de Génétique Médicale UCL
Alzheimer disease (gene panel)	APP, PSEN1, PSEN2, APOE		Early-onset autosomal dominant Alzheimer disease, Behavioral variant of frontotemporal dementia, Semantic dementia, Progressive non-fluent aphasia	Centre de Génétique Humaine - Erasme ULB
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

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