Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) (hot spot mutation - m.3243A>G)	MT-TL1		MELAS	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Diabetes, mitochondrial (hot spot mutation - m.3243A>G, MTTL1 (tRNA-Leu) )	MT-TL1		MELAS	Centrum Medische Genetica - UZ Antwerpen
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) (full sequencing)	MT-TL1		MELAS	Centrum Medische Genetica - UZ Brussel VUB
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) (hot spot mutation - m.3243A>G)	MT-TL1		MELAS	Centrum Medische Genetica - UZ Brussel VUB
Mitochondrial NeuroGastroIntestinal Encephalomyopathy (MNGIE) syndrome	TYMP, POLG, POLG2, RRM2B	MNGIE syndrome (4 genes) - VUB	Mitochondrial neurogastrointestinal encephalomyopathy	Centrum Medische Genetica - UZ Brussel VUB
Ocular albinism and oculocutaneous albinism type 1, 2, 3, 4, 6, 7, 8 (gene panel)	TYR, OCA2, TYRP1, SLC45A2, SLC24A5, LRMDA, GPR143	Ocular and oculocutaneous albinism - UGent	Oculocutaneous albinism type 1A, Oculocutaneous albinism type 1B, Oculocutaneous albinism type 2, Oculocutaneous albinism type 3, Oculocutaneous albinism type 4, Oculocutaneous albinism type 6, Oculocutaneous albinism type 7	Centrum Medische Genetica - UZ Gent
Segawa syndrome (TH gene)	TH		Autosomal recessive dopa-responsive dystonia	Centrum Medische Genetica - UZ Brussel VUB

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