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Stickler syndrome (gene panel)
Stickler syndrome - UGent
Stickler syndrome type 1
,
Stickler syndrome type 2
,
Autosomal dominant otospondylomegaepiphyseal dysplasia
Centrum Medische Genetica - UZ Gent
Chronic progressive external ophthalmoplegia (CPEO) (Full sequencing of mtDNA genome)
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Centrum Medische Genetica - UZ Brussel VUB
Mitochondrial disorders, mitchondrial DNA based (Full sequencing of mtDNA genome)
mitochondrial disorders, mitochondrial DNA based / mtDNA resequencing - VUB
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
,
Autosomal dominant progressive external ophthalmoplegia
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Autosomal recessive progressive external ophthalmoplegia
,
Isolated cytochrome C oxidase deficiency
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Maternally-inherited diabetes and deafness
,
Kearns-Sayre syndrome
,
Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure
,
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
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Mitochondrial DNA depletion syndrome, myopathic form
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Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
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Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies
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Mitochondrial DNA depletion syndrome, hepatocerebrorenal form
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Proximal myopathy with focal depletion of mitochondria
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Pearson syndrome
Centrum Medische Genetica - UZ Brussel VUB
Long QT syndrome
Long QT syndrome - UGent
Brugada syndrome
,
Romano-Ward syndrome
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Familial atrial fibrillation
Centrum Medische Genetica - UZ Gent
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