Genetic tests

Full name Analytes Gene panels Disease Laboratory
Uniparental Disomy (UDP7; UDP11; UDP14; UDP15; UDP16) Paternal uniparental disomy of chromosome 7, Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7, Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11, Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11, Temple syndrome due to maternal uniparental disomy of chromosome 14, Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14, Angelman syndrome due to paternal uniparental disomy of chromosome 15, Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15, Maternal uniparental disomy of chromosome 16 Centrum Medische Genetica - UZ Gent
Uniparental Disomy (UDP7; UDP11; UDP14; UDP20) Paternal uniparental disomy of chromosome 7, Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7, Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11, Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11, Temple syndrome due to maternal uniparental disomy of chromosome 14, Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14 Centrum Menselijke Erfelijkheid - KUL
Uniparental disomy 7p12.1, 7q32.2 Silver-Russell syndrome Centre de Génétique Médicale UCL
Uniparental Disomy Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Corneal dystrophy (gene panel) Corneal dystrophy - UGent Centrum Medische Genetica - UZ Gent
Intellectual disability (virtual gene panel) Intellectual disability (gene panel) Centre de Génétique Médicale UCL
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
Hereditary Spastic Paraplegia (gene panel) Hereditary Spastic Paraplegia & ataxia (genepanel) - UZA Centrum Medische Genetica - UZ Antwerpen
Myopathy (gene panel) Myopathy (genepanel) - UZA Centrum Medische Genetica - UZ Antwerpen
Peripheral neuropathy (gene panel) Neuropathy (genepanel) - UZA Centrum Medische Genetica - UZ Antwerpen
Primary ciliary dyskinesia (PCD) Heterotaxyies (gene panel) Heterotaxie PCD - UGent Centrum Medische Genetica - UZ Gent
Skeletal dysplasia (gene panel) Skeletal dysplasia - UGent Centrum Medische Genetica - UZ Gent
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
Pediatric oncopredisposition (gene panel) Pediatric oncopredisposition - UGent Centrum Medische Genetica - UZ Gent
Endocrine Disorders - Hypothyroidism (gene panel - 42 genes) Endocrine Disorders - Hypothyroidism (42 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Endocrine Disorders - Hyper(Hypo)parathyroidism (gene panel - 24 genes) Endocrine Disorders - Hyper(Hypo)parathyroidism (24 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Telomeropathies (virtual gene panel) Centre de Génétique Médicale UCL
Hepatology (gene panel) Hepatology panel - UGent Centrum Medische Genetica - UZ Gent
Respiratory disorders (gene panel): non-CF bronchiectasis; pulmonary hypertension; interstitial lung disease Respiratory Disorders panel (137 genes) - Ugent Centrum Medische Genetica - UZ Gent
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
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