Genetic tests |

Full name	Analytes	Gene panels	Disease	Laboratory
Lymphoproliferative syndrome, X-linked (SH2D1A gene) / Duncan's disease	SH2D1A		X-linked lymphoproliferative disease, X-linked lymphoproliferative disease due to SH2D1A deficiency	Centrum Menselijke Erfelijkheid - KUL
Lymphoproliferative syndrome, X-linked (XIAP gene)	XIAP		X-linked lymphoproliferative disease, X-linked lymphoproliferative disease due to XIAP deficiency	Centrum Menselijke Erfelijkheid - KUL
Alport autosomal recessive and X-linked and hematuria (3 genes)	COL4A3, COL4A4, COL4A5	Alport (X-linked and recessive) (3 genes) - IPG	Autosomal recessive Alport syndrome, X-linked Alport syndrome	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Gilbert syndrome (homozygous A(TA)7TAA allele)	UGT1A1		Gilbert syndrome (NON RARE IN EUROPE)	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Gilbert syndrome / Irinotecan sensitivity (homozygous A(TA)7TAA allele) - Pharmacogenetics	UGT1A1		Gilbert syndrome (NON RARE IN EUROPE), Irinotecan toxicity	Centre de Génétique Humaine - Erasme ULB
Gilbert disease / Irinotecan sensitivity / Raltegravir toxicity - Pharmacogenetics	UGT1A1		Gilbert syndrome (NON RARE IN EUROPE), Irinotecan toxicity	Centre de Génétique Humaine - CHU Sart-Tilman
Gilbert syndrome / Irinotecan sensitivity (homozygous A(TA)7TAA allele)	UGT1A1		Gilbert syndrome (NON RARE IN EUROPE), Irinotecan toxicity, Transient familial neonatal hyperbilirubinemia	Centrum Menselijke Erfelijkheid - KUL