Genetic tests |

Full name	Analytes	Gene panels	Disease	Laboratory
Congenital hemangioma (2 genes)	GNAQ, GNA11		Familial multiple nevi flammei, Sturge-Weber syndrome, Uveal melanoma	Centrum Menselijke Erfelijkheid - KUL
Melanoma (6 genes)	BAP1, CDK4, CDKN2A, MC1R, MITF, POT1	Melanoma (6 genes) - UCL	Familial melanoma, MITF-related melanoma and renal cell carcinoma predisposition syndrome, Uveal melanoma, Melanoma of soft tissue	Centre de Génétique Médicale UCL
Hyperthyroidism ( familial gestational or familial nonautoimmune, hypothyroidism, thyrotropin) - TSHR	TSHR		Familial hyperthyroidism due to mutations in TSH receptor, Hypothyroidism due to TSH receptor mutations, Familial gestational hyperthyroidism	Centre de Génétique Humaine - Erasme ULB
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