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
Reset
Full name
Analytes
Gene panels
Disease
Laboratory
Zygosity (medical)
Centrum Menselijke Erfelijkheid - KUL
Zygosity (medical)
Centre de Génétique Humaine - CHU Sart-Tilman
Zygosity (medical)
Centrum Medische Genetica - UZ Gent
X-linked Opitz G/BBB syndrome
MID1
X-linked Opitz G/BBB syndrome
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
X-linked hydrocephalia / CRASH (corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraplegia, and hydrocephalus) syndrome (L1CAM gene)
L1CAM
Hydrocephalus with stenosis of the aqueduct of Sylvius
Centrum Medische Genetica - UZ Brussel VUB
X-linked creatine deficiency
SLC6A8
X-linked creatine transporter deficiency
Centre de Génétique Humaine - CHU Sart-Tilman
X-linked agammaglobulinemia
BTK
X-linked agammaglobulinemia
Centrum Menselijke Erfelijkheid - KUL
X-chromosome inactivation
Centrum Medische Genetica - UZ Brussel VUB
X-chromosome inactivation
Centrum Menselijke Erfelijkheid - KUL
X-chromosome inactivation
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Wiskott-Aldrich syndrome
WAS
Wiskott-Aldrich syndrome
Centrum Menselijke Erfelijkheid - KUL
Wilson Disease
ATP7B
Wilson disease
Centre de Génétique Médicale UCL
Wilms tumor (DICER1; WT1 genes)
WT1
,
DICER1
Wilms' tumor (2 genes) - KUL
Centrum Menselijke Erfelijkheid - KUL
Whole exome sequencing
Centre de Génétique Médicale UCL
WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome
CXCR4
WHIM syndrome
Centrum Menselijke Erfelijkheid - KUL
Weill-Marchesani syndrome
Weill-Marchesani - UGent
Weill-Marchesani syndrome
Centrum Medische Genetica - UZ Gent
WAGR Syndrome
WT1
WAGR syndrome
Centrum Menselijke Erfelijkheid - KUL
Waardenburg Syndrome types I and III
PAX3
Waardenburg syndrome type 1
,
Waardenburg syndrome type 3
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Waardenburg syndrome (gene panel)
EDN3
,
EDNRB
,
MITF
,
PAX3
,
SNAI2
,
SOX10
Waardenburg syndrome (6 genes) - UZA
Waardenburg syndrome type 1
,
Waardenburg syndrome type 2
,
Waardenburg syndrome type 3
,
Waardenburg-Shah syndrome
Centrum Medische Genetica - UZ Antwerpen
Von Willebrand disease
VWF
Von Willebrand disease type 1
,
Von Willebrand disease type 2A
,
Von Willebrand disease type 2M
,
Von Willebrand disease type 2B
,
Von Willebrand disease type 2N
,
Von Willebrand disease type 3
Centrum Medische Genetica - UZ Antwerpen
Pagination
Current page
1
Page
2
Page
3
Page
4
Page
5
Page
6
Page
7
Page
8
Page
9
Next page
Next ›
Last page
Last »
Download XLSX
Download PDF
Did not find what you were looking for? Contact us through the support center.
Read more