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Achromatopsia
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IBMDx study
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Incidentalome_PREGEN_DRAFT
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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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Tubulinopathies
Usher Syndrome
Vascular Malformations_Germline
Vascular Malformations_Somatic
Vascular Malformations SuperPanel
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
Version
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1.0
0.272
Gene or Genomic Entity Name
TCF4_FECD3_CTG
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14 Apr 2026
Repeat Disorders v1.0
TCF4_FECD3_CTG
STR TCF4_FECD3_CTG: gene migrated from ENSG00000196628 to ENSG00000196628 (gene set migration)
24 Apr 2025
Repeat Disorders v0.186
TCF4_FECD3_CTG
Bryony Thompson FECD3 was changed to TCF4_FECD3_CTG