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Achromatopsia
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Alagille syndrome
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IBMDx study
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Liverome Superpanel
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Pierre Robin Sequence
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Prepair 1000+
Prepair 500+
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Retinal Disorders Superpanel
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Tubulinopathies
Usher Syndrome
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Vascular Malformations SuperPanel
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
Version
Panel Version
1.0
0.77
Gene or Genomic Entity Name
CCN2
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07 Jun 2026
Immune_markers_WTS_UMCCR v1.0
CCN2
Gene symbol changed from CTGF to CCN2 during gene set migration (ENSG00000118523 -> ENSG00000118523)