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Achromatopsia
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Alagille syndrome
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Deafness_IsolatedAndComplex
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Genomic newborn screening: BabyScreen+
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IBMDx study
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Incidentalome_PREGEN_DRAFT
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Kabuki syndrome
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Kidneyome_SuperPanel
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Limb and Digital Malformations SuperPanel
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Lipodystrophy_Lipoatrophy
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Liver Failure_Paediatric
Liverome Superpanel
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Mackenzie's Mission_Reproductive Carrier Screening
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Multiple pterygium syndrome_Fetal akinesia sequence
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Myopathy Superpanel
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Photosensitivity Syndromes
Pierre Robin Sequence
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Prepair 1000+
Prepair 500+
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Prostate Cancer
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Renal Cystic Disease_SuperPanel
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Retinal Disorders Superpanel
Retinitis pigmentosa
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Severe Combined Immunodeficiency
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Short QT syndrome
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Speech apraxia
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Stickler Syndrome
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Thyroid Cancer
Transplant Co-Morbidity
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly
Tubulinopathies
Usher Syndrome
Vascular Malformations_Germline
Vascular Malformations_Somatic
Vascular Malformations SuperPanel
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
Version
Panel Version
2.0
1.29
Gene or Genomic Entity Name
LYSET
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07 Jun 2026
Arthrogryposis v2.0
LYSET
Gene symbol changed from TMEM251 to LYSET during gene set migration (ENSG00000153485 -> ENSG00000153485)