Genetic tests | Belgian Genetic Tests database

Statistics

Type	Total	Last update
Genetic tests	859	2024-02-16
Diseases	4232	2023-06-22
Analytes	6169	2023-12-20
Gene panels	380	2024-03-20

Full name	Analytes	Gene panels	Disease	Laboratory
Charcot-Marie-Tooth type 1A / Hereditary Neuropathy with Liability to Pressure Palsies	PMP22		Charcot-Marie-Tooth disease type 1A, Hereditary neuropathy with liability to pressure palsies	Centrum Medische Genetica - UZ Gent
Charcot-Marie-Tooth type 1A (CMT1A) / Hereditary Neuropathy with Liability to Pressure Palsies	PMP22		Charcot-Marie-Tooth disease type 1A, Hereditary neuropathy with liability to pressure palsies	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Charcot-Marie-Tooth type 1A / Hereditary Neuropathy with Liability to Pressure Palsies	PMP22		Charcot-Marie-Tooth disease type 1A, Hereditary neuropathy with liability to pressure palsies, Charcot-Marie-Tooth disease type 1E	Centrum Medische Genetica - UZ Antwerpen
Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)	PMP22		Charcot-Marie-Tooth disease type 1A, Hereditary neuropathy with liability to pressure palsies	Centre de Génétique Humaine - Erasme ULB
Charcot-Marie-Tooth type 1A (CMT1A) / Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)	PMP22		Charcot-Marie-Tooth disease type 1A, Dejerine-Sottas syndrome, Hereditary neuropathy with liability to pressure palsies	Centrum Menselijke Erfelijkheid - KUL
Charcot-Marie-Tooth type 1A / Hereditary Neuropathy with Liability to Pressure Palsies	PMP22		Charcot-Marie-Tooth disease type 1A, Hereditary neuropathy with liability to pressure palsies	Centre de Génétique Humaine - CHU Sart-Tilman
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

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