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Achromatopsia
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Incidentalome_PREGEN_DRAFT
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Kidneyome_SuperPanel
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Liverome Superpanel
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Myopathy Superpanel
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Pierre Robin Sequence
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Prepair 1000+
Prepair 500+
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Renal Cystic Disease_SuperPanel
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Retinal Disorders Superpanel
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Short QT syndrome
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Tubulinopathies
Usher Syndrome
Vascular Malformations_Germline
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Vascular Malformations SuperPanel
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
Version
Panel Version
1.0
0.280
Gene or Genomic Entity Name
GSDME
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07 Jun 2026
Additional findings_Paediatric v1.0
GSDME
Gene symbol changed from DFNA5 to GSDME during gene set migration (ENSG00000105928 -> ENSG00000105928)