Genetic tests

Full name Analytes Gene panels Disease Laboratory
Thyroid hormone receptor resistance (THRB gene) THRB Pituitary resistance to thyroid hormone, Generalized resistance to thyroid hormone Centrum Medische Genetica - UZ Brussel VUB
Dihydropyrimidine dehydrogenase deficiency (5-fluorouracil (5-FU) toxicity) - Pharmacogenetics DPYD 5-fluorouracil toxicity, Dihydropyrimidine dehydrogenase deficiency Centre de Génétique Humaine - CHU Sart-Tilman
Dihydropyrimidine dehydrogenase deficiency; 5-fluorouracil toxicity - pharmacogenetics (4 variants: DPYD*2A, DPYD*13, c.2846A>T, HapB3) - Pharmacogenetics DPYD Dihydropyrimidine dehydrogenase deficiency Centrum Medische Genetica - UZ Gent
Dihydropyrimidine dehydrogenase deficiency/5-fluorouracil toxicity - Pharmacogenetics (4 variants: DPYD*2A, DPYD*13, c.2846A>T, HapB3) DPYD Dihydropyrimidine dehydrogenase deficiency Centrum Menselijke Erfelijkheid - KUL
Carnitine Palmitoyltransferase type II CPT2 Carnitine palmitoyl transferase II deficiency, myopathic form, Carnitine palmitoyl transferase II deficiency, severe infantile form, Carnitine palmitoyl transferase II deficiency, neonatal form Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Carnitine Palmitoyl transferase type II CPT2 Carnitine palmitoyl transferase II deficiency, severe infantile form, Carnitine palmitoyl transferase II deficiency, neonatal form, Carnitine palmitoyl transferase II deficiency, myopathic form Centrum Medische Genetica - UZ Antwerpen
Birt-Hogg-Dubé syndrome FLCN Birt-Hogg-Dubé syndrome Centrum Medische Genetica - UZ Gent
Birt-Hogg-Dubé syndrome FLCN Birt-Hogg-Dubé syndrome Centrum Menselijke Erfelijkheid - KUL
Birt-Hogg-Dubé syndrome FLCN Birt-Hogg-Dubé syndrome Centre de Génétique Médicale UCL
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