Genetic tests

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Full name	Analytes	Gene panels	Disease	Laboratory
Hirschsprung disease		Hirschsprung disease - Ugent	Hirschsprung disease	Centrum Medische Genetica - UZ Gent
Multiple Endocrine Neoplasia type 2A and 2B / Familial medullary thyroid carcinoma	RET		Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia type 2B, Familial medullary thyroid carcinoma, Hirschsprung disease	Centrum Medische Genetica - UZ Gent
Hirschsprung disease	RET		Hirschsprung disease	Centrum Menselijke Erfelijkheid - KUL
Hirschsprung disease	RET		Hirschsprung disease	Centre de Génétique Médicale UCL
Arteriovenous malformation (gene panel)		Arteriovenous malformation (7 genes), Vascular malformations (germline) (38 genes) - UCL	Hereditary hemorrhagic telangiectasia, Heritable pulmonary arterial hypertension, Familial cerebral saccular aneurysm, Vein of Galen aneurysmal malformation, Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome, Capillary malformation-arteriovenous malformation, Parkes Weber syndrome, Microcephaly-capillary malformation syndrome	Centre de Génétique Médicale UCL
Capillary malformation – microcephaly	STAMBP		Microcephaly-capillary malformation syndrome	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