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
Von Hippel Lindau	VHL		Von Hippel-Lindau disease	Centrum Menselijke Erfelijkheid - KUL
Von Hippel Lindau syndrome	VHL		Von Hippel-Lindau disease	Centrum Medische Genetica - UZ Gent
Paraganglioma-pheochromocytoma (6 genes) - ULG	RET, VHL, SDHA, SDHB, SDHC, SDHD	Paraganglioma-pheochromocytoma (6 genes) - ULG	Hereditary pheochromocytoma-paraganglioma, Von Hippel-Lindau disease, Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia type 2A	Centre de Génétique Humaine - CHU Sart-Tilman
Von Hippel Lindau disease	VHL		Von Hippel-Lindau disease	Centre de Génétique Médicale UCL
Hallervorden-Spatz disease (Neurodegeneration with brain iron accumulation type 1) / HARP syndrome (Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis pigmentosa, and Pallidal degeneration)	PANK2		Classic pantothenate kinase-associated neurodegeneration, Atypical pantothenate kinase-associated neurodegeneration	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Pituitary adenoma (5 genes)	AIP, CDKN1B, MEN1, RET, PRKAR1A	Pituitary adenoma (5 genes) - UCL	Familial isolated pituitary adenoma, Silent pituitary adenoma, Null pituitary adenoma, Prolactinoma, Pituitary gigantism, Acromegaly	Centre de Génétique Médicale UCL
Lissencephaly / subcortical band heterotopia	PAFAH1B1		Lissencephaly due to LIS1 mutation, Subcortical band heterotopia	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Lissencephaly, X-linked / subcortical band heterotopia	DCX		Lissencephaly type 1 due to doublecortin gene mutation, Subcortical band heterotopia	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Malformations of cortical development (235 genes)		Malformations of cortical development (235 genes) - VUB	Bilateral perisylvian polymicrogyria, Cobblestone lissencephaly without muscular or ocular involvement, Lissencephaly due to LIS1 mutation, Lissencephaly due to TUBA1A mutation, Lissencephaly syndrome, Norman-Roberts type, Lissencephaly type 1 due to doublecortin gene mutation, Microlissencephaly, Polymicrogyria due to TUBB2B mutation, Subcortical band heterotopia, X-linked lissencephaly with abnormal genitalia	Centrum Medische Genetica - UZ Brussel VUB

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