Genetic tests

Full name Analytes Gene panels Disease Laboratory
Adams-Oliver syndrome (gene panel) ARHGAP31, DOCK6, RBPJ, NOTCH1, DLL4, EOGT Adams-Oliver (6 genes) - UZA Adams-Oliver syndrome Centrum Medische Genetica - UZ Antwerpen
Amyotrophic Lateral Sclerosis (ALS) (gene panel) Amyotrophic Lateral Sclerosis (ALS) - UGent Amyotrophic lateral sclerosis, Juvenile amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis type 4 Centrum Medische Genetica - UZ Gent
Aneurysm, Thoracic Aortic, familial (gene panel) Familial Thoracic Aortic Aneurysm (genepanel) - UZA Familial thoracic aortic aneurysm and aortic dissection Centrum Medische Genetica - UZ Antwerpen
Ataxia (autosomic dominant and recessive / except expansion of triplets) (gene panel - 722 genes) Ataxia (348 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Ataxia Spasticity (gene panel) Ataxia Spasticity - UGent Centrum Medische Genetica - UZ Gent
Cardiomyopathy: hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy, left ventricular non-compaction cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy (gene panel) Cardiomyopathy (genepanel) - UZA Familial isolated dilated cardiomyopathy, Familial isolated restrictive cardiomyopathy, Left ventricular noncompaction, Familial isolated arrhythmogenic ventricular dysplasia, right dominant form Centrum Medische Genetica - UZ Antwerpen
Cataract (gene panel) Cataract - UGent Centrum Medische Genetica - UZ Gent
Cerebral palsy (gene panel) Cerebral palsy (212 genes) - UZA Centrum Medische Genetica - UZ Antwerpen
Charcot-Marie-Tooth type 1A / Hereditary Neuropathy with Liability to Pressure Palsies PMP22 Charcot-Marie-Tooth disease type 1A, Hereditary neuropathy with liability to pressure palsies, Charcot-Marie-Tooth disease type 1E Centrum Medische Genetica - UZ Antwerpen
Ciliopathy (gene panel) Ciliopathy (120 genes) - UGent Centrum Medische Genetica - UZ Gent
cleft lip with/whitout cleft palate (virtual gene panel) Cleft lip and palate / dysmorphic facial features / craniofacial anomalies (255 genes)) - UCL Cleft lip/palate Centre de Génétique Médicale UCL
Congenital malformation (gene panel - 1721 genes) Congenital malformation (1721 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Congenital structural heart defects (gene panel) Congenital structural heart defects - UGent Centrum Medische Genetica - UZ Gent
Corneal dystrophy (gene panel) Corneal dystrophy - UGent Centrum Medische Genetica - UZ Gent
Craniosynostosis (gene panel) Craniosynostosis (32 genes) - KUL Centrum Menselijke Erfelijkheid - KUL
Craniosynostosis (gene panel) Craniosynostosis (UZ Gent) Centrum Medische Genetica - UZ Gent
Dementia, young onset (gene panel) Dementia, young onset (gene panel) Centrum Medische Genetica - UZ Antwerpen
Dermatogenetic panel, severe, rare and hereditary genodermatoses (gene panel - 394 genes) Dermatogenetic / severe, rare and hereditary genodermatoses (394 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Developmental disorders: intellectual disability and multiple congenital anomalies (gene panel) Developmental disorders: intellectual disability and multiple congenital anomalies (gene panel) - KUL Centrum Menselijke Erfelijkheid - KUL
Disorders of sex development - Primary Ovarian insufficiency - Hypogonadotropic Hypogonadism (gene panel) Disorders of Sex Development - Primary Ovarian Insufficiency - Hypogonadotropic Hypogonadism - UGent Centrum Medische Genetica - UZ Gent
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