Genetic tests | Belgian Genetic Tests database

Statistics

Type	Total	Last update
Genetic tests	859	2024-02-16
Diseases	4232	2023-06-22
Analytes	6169	2023-12-20
Gene panels	380	2024-03-20

Full name	Analytes	Gene panels	Disease	Laboratory
Kennedy disease (Spinal and bulbar muscular atrophy, SBMA) - CAG repeat expansion	AR		Kennedy disease	Centrum Menselijke Erfelijkheid - KUL
Kennedy disease (Spinal and bulbar muscular atrophy, SBMA) - CAG repeat expansion	AR		Kennedy disease	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Kennedy disease (Spinal and bulbar muscular atrophy, SBMA) - CAG repeat expansion	AR		Kennedy disease	Centrum Medische Genetica - UZ Antwerpen
Androgen insensitivity (AR gene)	AR		Partial androgen insensitivity syndrome, Complete androgen insensitivity syndrome	Centrum Medische Genetica - UZ Brussel VUB
Kennedy disease / Spinal and bulbar muscular atrophy (SBMA) - AR gene CAG repeat expansion	AR		Kennedy disease	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
Charcot-Marie-Tooth (CMT1A, GJB1)	GJB1, PMP22		X-linked Charcot-Marie-Tooth disease type 1, Charcot-Marie-Tooth disease type 1A	Centre de Génétique Humaine - Erasme ULB
Medium chain acyl-CoA dehydrogenase deficiency (MCAD hot spot mutation - p.Lys329Glu)	ACADM		Medium chain acyl-CoA dehydrogenase deficiency	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Medium chain acyl-CoA dehydrogenase deficiency (MCAD-ACADM)	ACADM		Medium chain acyl-CoA dehydrogenase deficiency	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Medium chain acyl-CoA dehydrogenase deficiency (MCAD-ACADM gene)	ACADM		Medium chain acyl-CoA dehydrogenase deficiency	Centrum Medische Genetica - UZ Brussel VUB
Medium chain acyl-CoA dehydrogenase deficiency (MCAD hot spot mutation - p.Lys329Glu)	ACADM		Medium chain acyl-CoA dehydrogenase deficiency	Centre de Génétique Humaine - CHU Sart-Tilman

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