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Analytes
Gene panels
Disease
Laboratory
Metastatic Breast or Pancreatic or Prostate Cancer
BRCA1
,
BRCA2
Centrum Menselijke Erfelijkheid - KUL
« Inherited bone marrow failures syndromes » with or without organ dysfunction
Hematologic Familiar Forms - ULG
Centre de Génétique Humaine - CHU Sart-Tilman
Immunodysregulation - polyendocrinopathy - enteropathy - X-linked (IPEX) syndrome
FOXP3
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
Centrum Menselijke Erfelijkheid - KUL
Telomeropathies (virtual gene panel)
Centre de Génétique Médicale UCL
Hereditary cancer panel (gene panel)
Hereditary Cancer Solution (35 genes) - UCL
Centre de Génétique Médicale UCL
Hereditary Polyposis Panel (11 genes) - ULG
APC
,
MUTYH
,
BMPR1A
,
NTHL1
,
SMAD4
,
MSH3
,
POLE
,
POLD1
,
PTEN
,
STK11
,
GREM1
Hereditary Polyposis Panel (11 genes) - ULG
Familial adenomatous polyposis
,
MUTYH-related attenuated familial adenomatous polyposis
,
Turcot syndrome with polyposis
,
Hereditary mixed polyposis syndrome
,
Generalized juvenile polyposis/juvenile polyposis coli
Centre de Génétique Humaine - CHU Sart-Tilman
Hereditary Melanoma Panel (7 genes)
CDKN2A
,
CDK4
,
POT1
,
TERT
,
TERF2IP
,
BAP1
,
MITF
Hereditary Melanoma Panel (7 genes) - ULG
Familial melanoma
Centre de Génétique Humaine - CHU Sart-Tilman
Germline analysis of BRCA1/2 for iPARP treatment
BRCA1
,
BRCA2
Germline analysis of BRCA1/2 for iPARP treatment
Hereditary breast cancer
Centre de Génétique Humaine - CHU Sart-Tilman
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
Arrhytmogenic cardiopathy
Arrhytmogenic cardiopathy - UGent
Centrum Medische Genetica - UZ Gent
Dilated cardiomyopathy
Dilated cardiomyopathy - UGent
Centrum Medische Genetica - UZ Gent
VEXAS-syndrome
UBA1
VEXAS syndrome
Centrum Medische Genetica - UZ Gent
Supravalvular aortic stenosis
ELN
Centrum Medische Genetica - UZ Gent
Hirschsprung disease
Hirschsprung disease - Ugent
Hirschsprung disease
Centrum Medische Genetica - UZ Gent
Small cell carcinoma of the ovary
SMARCA4
Small cell carcinoma of the ovary
Centrum Medische Genetica - UZ Gent
Movement Disorders (gene panel)
Movement Disorders - ULG
Centre de Génétique Humaine - CHU Sart-Tilman
Keratinopathic ichthyosis (epidermolytic ichtyosis, superficial epidermolytic ichthyosis, congenital reticular ichthyosiform erythroderma) (3 genes)
keratinopathic ichthyosis (3 genes) - KUL
Autosomal dominant epidermolytic ichthyosis
,
Superficial epidermolytic ichthyosis
,
Congenital reticular ichthyosiform erythroderma
Centrum Menselijke Erfelijkheid - KUL
Dementia, young onset (gene panel)
Dementia, young onset (gene panel)
Centrum Medische Genetica - UZ Antwerpen
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