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Rett syndrome
MECP2
Rett syndrome
,
Atypical Rett syndrome
Centre de Génétique Humaine - CHU Sart-Tilman
Hypogonadotropic hypogonadism (33 genes)
Hypogonadotropic hypogonadism (33 genes) - VUB
Normosmic congenital hypogonadotropic hypogonadism
Centrum Medische Genetica - UZ Brussel VUB
Kallmann syndrome / Hypogonadotropic Hypogonadism (FGFR1 gene)
FGFR1
Kallmann syndrome
,
Normosmic congenital hypogonadotropic hypogonadism
Centre de Génétique Humaine - CHU Sart-Tilman
Alzheimer Disease, late onset (AD2) / ApoE2, E3, and E4 isoforms
APOE
Alzheimer disease (NON RARE IN EUROPE)
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Alzheimer Disease, late onset (AD2) / ApoE2, E3, and E4 isoforms
APOE
Alzheimer disease (NON RARE IN EUROPE)
Centrum Menselijke Erfelijkheid - KUL
Alzheimer Disease, late onset (AD2) / ApoE2, E3, and E4 isoforms
APOE
Alzheimer disease (NON RARE IN EUROPE)
Centre de Génétique Humaine - CHU Sart-Tilman
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
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