Genetic tests

Full name Analytes Gene panels Disease Laboratory
Neurodevelopmental disorders (1300 genes) Neurodevelopmental disorders (1300 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Dyslipidemia (gene panel) Dyslipidemia ( 13 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
Prostate cancer susceptibility (7 genes) Prostate cancer susceptibility (7 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Amyloidosis hereditary (gene panel) Amyloidosis (3 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Endocrine Disorders - Hypothyroidism (gene panel - 42 genes) Endocrine Disorders - Hypothyroidism (42 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Ataxia (autosomic dominant and recessive / except expansion of triplets) (gene panel - 722 genes) Ataxia (348 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Thalassemia Alpha (2 genes) HBA1, HBA2 Thalassemia Alpha (2 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Pulmonary Arterial Hypertension / Rendu Osler Weber disease (gene panel - 24 genes) Pulmonary Arterial Hypertension (24 genes) - ULB Centre de Génétique Humaine - Erasme ULB
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
Porphyria (10 genes) Porphyria (10 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Early onset epileptic encephalopathy (gene panel - 845 genes) Early onset epileptic encephalopathy (845 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Hemochromatosis (17 genes) Hemochromatosis (17 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Hereditary Hemolytic Anemias due to unknown or doubtful origin (gene panel - 52 genes) Hereditary Hemolytic Anemias (52 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Hereditary spastic paraplegia (gene panel - 249 genes) Hereditary spastic paraplegia (188 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Periodic Fever (88 genes) Periodic Fever (88 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Neuromuscular disorders (548 genes) Neuromuscular disorders (548 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Congenital malformation (gene panel - 1721 genes) Congenital malformation (1721 genes) - ULB Centre de Génétique Humaine - Erasme ULB
Achondroplasia (hot spot mutation - p.Gly380) FGFR3 Achondroplasia Centre de Génétique Humaine - Erasme ULB
Angelman / Prader Willi Syndrome 15q11-q13, UBE3A Angelman syndrome due to imprinting defect in 15q11-q13, Angelman syndrome due to maternal 15q11q13 deletion, Prader-Willi syndrome due to imprinting mutation, Angelman syndrome due to paternal uniparental disomy of chromosome 15, Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2, Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15, Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1 Centre de Génétique Humaine - Erasme ULB
Download XLSX
Download PDF