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
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
Leigh syndrome	COX15		Leigh syndrome with leukodystrophy, Leigh syndrome with cardiomyopathy	Centrum Medische Genetica - UZ Brussel VUB
Obesity (gene panel)	ADCY3, BDNF, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, SIM1, UCP3	Obesitas (genepanel) - UZA		Centrum Medische Genetica - UZ Antwerpen
Obesitas, early onset (gene panel)	MC4R, MC3R, LEP, LEPR, PCSK1, POMC, SIM1, NTRK2	Obesitas, early onset (8 genes) - VUB		Centrum Medische Genetica - UZ Brussel VUB
Obesitas, Monogenic early onset	MC4R		Obesity due to melanocortin 4 receptor deficiency	Centre de Génétique Humaine - CHU Sart-Tilman

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