Skip to main content
Log in
Sciensano
Support
Belgian Genetic Tests database
Toggle navigation
Main navigation
Home
Genetic tests
Analytes
Diseases
Labs
Guide
Contact
Genetic tests
20
50
100
Search
Full name
Analytes
Gene panels
Disease
Laboratory
Bile Acid Synthesis Congenital Defect (gene panel)
AKR1D1
,
AMACR
,
CYP7B1
,
HSD3B7
,
CYP27A1
Bile Acid Synthesis Congenital Defect (5 genes) - UCL
Congenital bile acid synthesis defect type 2
,
Congenital bile acid synthesis defect type 4
,
Cerebrotendinous xanthomatosis
,
Congenital bile acid synthesis defect type 3
,
Congenital bile acid synthesis defect type 1
Centre de Génétique Médicale UCL
X-linked agammaglobulinemia
BTK
X-linked agammaglobulinemia
Centrum Menselijke Erfelijkheid - KUL
Overgrowth & vascular anomalies / CLOVES syndrome
PIK3CA
CLOVES syndrome
Centrum Menselijke Erfelijkheid - KUL
Vascular malformations (somatic)
AKT1
,
AKT2
,
AKT3
,
ALK
,
BRAF
,
GNA11
,
GNA14
,
GNAQ
,
HRAS
,
IDH1
,
IDH2
,
KRAS
,
NRAS
,
PIK3CA
,
PIK3R1
,
PIK3R2
,
PTEN
,
TEK
,
MAP3K3
,
MAP2K1
Vascular malformations (somatic) (19 genes) - UCL
Capillary malformation-arteriovenous malformation
,
CLOVES syndrome
,
Maffucci syndrome
,
Proteus syndrome
Centre de Génétique Médicale UCL
Long chain 3-hydroxyl-CoA dehydrogenase deficiency (hot spot mutation - p.Glu510Gln)
HADHA
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Download XLSX
Download PDF
Did not find what you were looking for? Contact us through the support center.
Read more