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
Dentatorubral pallidoluysian atrophy (DRPLA) - CAG repeat expansion	ATN1		Dentatorubral pallidoluysian atrophy	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Dentatorubral pallidoluysian atrophy (DRPLA) - CAG repeat expansion	ATN1		Dentatorubral pallidoluysian atrophy	Centrum Medische Genetica - UZ Antwerpen
Dentatorubral pallidoluysian atrophy - ATN1 gene CAG repeat expansion	ATN1		Dentatorubral pallidoluysian atrophy	Centrum Medische Genetica - UZ Brussel VUB
Spinocerebellar ataxia (type 8, 17) + Dentatorubral pallidoluysian atrophy - repeat expansion	ATXN8, TBP, ATN1	Spinocerebellar ataxia (type 8, 17 + ATN1) (5 genes) - VUB	Spinocerebellar ataxia type 8, Spinocerebellar ataxia type 17, Dentatorubral pallidoluysian atrophy	Centrum Medische Genetica - UZ Brussel VUB
Kennedy disease (Spinal and bulbar muscular atrophy, SBMA) - CAG repeat expansion	AR		Kennedy disease	Centrum Menselijke Erfelijkheid - KUL
Kennedy disease (Spinal and bulbar muscular atrophy, SBMA) - CAG repeat expansion	AR		Kennedy disease	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Kennedy disease (Spinal and bulbar muscular atrophy, SBMA) - CAG repeat expansion	AR		Kennedy disease	Centrum Medische Genetica - UZ Antwerpen
Kennedy disease / Spinal and bulbar muscular atrophy (SBMA) - AR gene CAG repeat expansion	AR		Kennedy disease	Centrum Medische Genetica - UZ Brussel VUB
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)
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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