Genetic tests

Full name Analytes Gene panels Disease Laboratory
Peutz-Jeghers Syndrome STK11 Peutz-Jeghers syndrome Centre de Génétique Médicale UCL
Peutz-Jeghers Syndrome (STK11 gene) STK11 Peutz-Jeghers syndrome Centre de Génétique Humaine - CHU Sart-Tilman
Ellis-van Creveld syndrome (2 genes) EVC, EVC2 Ellis-van Creveld (2 genes) - IPG Ellis Van Creveld syndrome Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
BAP1-related tumor predisposition syndrome (TPDS) BAP1 Familial melanoma Centrum Menselijke Erfelijkheid - KUL
Hereditary Melanoma Panel (7 genes) CDKN2A, CDK4, POT1, TERT, TERF2IP, BAP1, MITF Hereditary Melanoma Panel (7 genes) - ULG Familial melanoma Centre de Génétique Humaine - CHU Sart-Tilman
Familial melanoma / Familial Atypical Multiple Mole Melanoma Syndrome, FAMMM (gene panel) Familial melanoma - UGent Familial melanoma Centrum Medische Genetica - UZ Gent
Susceptibility to Cutaneous Malignant Melanoma CDK4 Familial melanoma Centre de Génétique Humaine - CHU Sart-Tilman
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
Macular dystrophy PRPH2 Butterfly-shaped pigment dystrophy Centrum Medische Genetica - UZ Gent
Microphthalmia, syndromic 5; Retinal dystrophy, early-onset, and pituitary dysfunction OTX2 Syndromic microphthalmia type 5, Combined pituitary hormone deficiencies, genetic forms, Butterfly-shaped pigment dystrophy Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
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