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Diamond Blackfan anaemia
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Dystonia_Superpanel
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IBMDx study
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Liverome Superpanel
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Multiple pterygium syndrome_Fetal akinesia sequence
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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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Retinal Disorders Superpanel
Retinitis pigmentosa_Autosomal Dominant
Retinitis pigmentosa_Autosomal Recessive/X-linked
Retinitis Pigmentosa Superpanel
Rhabdomyolysis and Metabolic Myopathy
Sarcoma non-soft tissue
Sarcoma soft tissue
Schwannoma
Severe Combined Immunodeficiency (absent T absent B cells)
Severe Combined Immunodeficiency (absent T present B cells)
Severe early-onset obesity
Short Long Bones with Advanced Carpal Bone Age
Short QT syndrome
Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy
Skeletal dysplasia
Skeletal Dysplasia_Fetal
Skeletal Muscle Channelopathies
Speech apraxia
Spondylocostal Dysostosis
Spontaneous coronary artery dissection
Stickler Syndrome
Stroke
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Susceptibility to Viral Infections
Syndromic Retinopathy
Thyroid Cancer
Transplant Co-Morbidity Superpanel
Tremors_Superpanel
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Tubulinopathies
Usher Syndrome
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Vascular Malformations_Somatic
Vascular Malformations SuperPanel
Vasculitis
Ventricular Fibrillation
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
Version
Panel Version
1.27
Gene or Genomic Entity Name
ZFHX3_SCA4_GGC
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27 Apr 2025
Hereditary Neuropathy - complex v1.27
ZFHX3_SCA4_GGC
Bryony Thompson SCA4_ZFHX3_GGC was changed to ZFHX3_SCA4_GGC