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Autoimmune lymphoproliferative syndrome, type V
CTLA4
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency
Centrum Menselijke Erfelijkheid - KUL
WAGR Syndrome
WT1
WAGR syndrome
Centrum Menselijke Erfelijkheid - KUL
Wilms tumor (DICER1; WT1 genes)
WT1
,
DICER1
Wilms' tumor (2 genes) - KUL
Centrum Menselijke Erfelijkheid - KUL
FRMD7-related infantile nystagmus / Nystagmus, infantile periodic alternating, X-linked
FRMD7
Nystagmus, infantile periodic alternating, X-linked
Centrum Medische Genetica - UZ Gent
ABCB1 genotyping (c.3435C>T, c.1199G>A ) - Transport protein - Pharmacogenetics
ABCB1
Resistance to colchicine
Centre de Génétique Médicale UCL
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