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Achromatopsia
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IBMDx study
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Incidentalome_PREGEN_DRAFT
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Kidneyome_SuperPanel
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Lipodystrophy_Lipoatrophy
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Liverome Superpanel
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Mackenzie's Mission_Reproductive Carrier Screening
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Muscular dystrophy and myopathy_Paediatric
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
Retinitis pigmentosa
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Short QT syndrome
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Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly
Tubulinopathies
Usher Syndrome
Vascular Malformations_Germline
Vascular Malformations_Somatic
Vascular Malformations SuperPanel
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
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2.0
1.44
Gene or Genomic Entity Name
DRC4
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14 Apr 2026
Heterotaxy v2.0
DRC4
Gene migrated from ENSG00000141013 to ENSG00000141013 (gene set migration)