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Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique Médicale UCL
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centrum Medische Genetica - UZ Gent
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centrum Medische Genetica - UZ Antwerpen
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique Humaine - Erasme ULB
Huntington disease - HTT gene CAG repeat expansion
HTT
Huntington disease
Centrum Medische Genetica - UZ Brussel VUB
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique Humaine - CHU Sart-Tilman
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centrum Menselijke Erfelijkheid - KUL
Hemophilia A
F8
Hemophilia A
,
Severe hemophilia A
,
Moderate hemophilia A
,
Mild hemophilia A
,
Bleeding disorder in hemophilia A carriers
Centre de Génétique Médicale UCL
Hemophilia A
F8
Hemophilia A
,
Mild hemophilia A
,
Severe hemophilia A
,
Moderate hemophilia A
,
Bleeding disorder in hemophilia A carriers
Centrum Menselijke Erfelijkheid - KUL
Temple syndrome / Kagami-Ogata Syndrome
DLK1
,
MEG3
,
RTL1
Temple syndrome due to maternal uniparental disomy of chromosome 14
,
Temple syndrome due to paternal 14q32.2 hypomethylation
,
Temple syndrome due to paternal 14q32.2 microdeletion
,
Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14
,
Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation
,
Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion
Centre de Génétique Médicale UCL
Autosomal dominant non-syndromic sensorineural deafness type DFNA9 (COCH partial sequencing)
COCH
Rare autosomal dominant non-syndromic sensorineural deafness type DFNA
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Deafness, autosomal dominant 6/14 / Wolfram syndrome
WFS1
Rare autosomal dominant non-syndromic sensorineural deafness type DFNA
,
Wolfram syndrome
Centrum Medische Genetica - UZ Antwerpen
Hearing loss (deafness), autosomal dominant 9 (COCH exons 4 and 5)
COCH
Rare autosomal dominant non-syndromic sensorineural deafness type DFNA
Centrum Medische Genetica - UZ Antwerpen
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