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Laboratory
Neurofibromatosis type 2
NF2
Full NF2-related schwannomatosis
Centrum Medische Genetica - UZ Gent
Primary cardiac arrhythmias (Atrial fibrillation / Brugada syndome / Catech. polymorphic ventricular tachycardia / Early repolaristion syndrome / Ideopathic ventricular fibrillation / Long QT syndrome / Sick sinus syndrome / Short QT syndrome) (gene pane)
AKAP9
,
ANK2
,
CACNA1C
,
CACNA2D1
,
CACNB2
,
CAV3
,
GPD1L
,
HCN4
,
KCNE1
,
KCNE2
,
KCNE3
,
KCNE5
,
KCNH2
,
KCNJ2
,
KCNJ8
,
KCNQ1
,
RANGRF
,
SCN10A
,
SCN1B
,
SCN2B
,
SCN3B
,
SCN4B
,
SCN5A
,
SLMAP
,
SNTA1
,
TRPM4
,
KCND3
,
KCNJ5
Primary cardiac arrhythmias (113 genes) - VUB
Andersen-Tawil syndrome
,
Brugada syndrome
,
Catecholaminergic polymorphic ventricular tachycardia
,
Early repolarization syndrome
,
Familial atrial fibrillation
,
Familial short QT syndrome
,
Familial sick sinus syndrome
,
Familial long QT syndrome
,
Idiopathic ventricular fibrillation, non Brugada type
,
Jervell and Lange-Nielsen syndrome
Centrum Medische Genetica - UZ Brussel VUB
Catecholaminergic polymorphic ventricular tachycardia (CPVT)
Catecholaminergic polymorphic ventricular tachycardia (CPVT) - UGent
Catecholaminergic polymorphic ventricular tachycardia
Centrum Medische Genetica - UZ Gent
Agammaglobulinemia
PIK3R1
Autosomal agammaglobulinemia
Centrum Menselijke Erfelijkheid - KUL
Dicer1 tumor predisposition syndrome
DICER1
Familial multinodular goiter
,
DICER1 tumor-predisposition syndrome
,
Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome
,
Malignant Sertoli-Leydig cell tumor of the ovary
,
Maligant granulosa cell tumor of the ovary
,
Gynandroblastoma
Centrum Medische Genetica - UZ Gent
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