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Achromatopsia
Additional findings_Adult
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Adult Cardiac SuperPanel
Alagille syndrome
Alternating Hemiplegia and Hemiplegic Migraine
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Deafness_IsolatedAndComplex
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Diamond Blackfan anaemia
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Ectodermal Dysplasia
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Haematuria_Alport
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Hereditary Pigmentary Disorders
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IBMDx study
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Immune_markers_WTS_UMCCR
Immunological disorders_SuperPanel
Imprinting disorders
Incidentalome
Incidentalome_PREGEN_DRAFT
Infertility and Recurrent Pregnancy Loss
Inflammatory bowel disease
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Joubert syndrome and other neurological ciliopathies
Kabuki syndrome
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Kidneyome_SuperPanel
Leukodystrophy
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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Movement Disorders Superpanel
Multiple pterygium syndrome_Fetal akinesia sequence
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Myopathy Superpanel
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Neuromuscular Superpanel
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Pharmacogenomics_Paediatric
Photosensitivity Syndromes
Pierre Robin Sequence
Pituitary hormone deficiency
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Pneumothorax
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Polymicrogyria and Schizencephaly
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Prepair 1000+
Prepair 500+
Primary nodular adrenocortical disease
Primary Ovarian Insufficiency_Premature Ovarian Failure
Progressive Myoclonic Epilepsy
Progressive Neurological Conditions
Prostate Cancer
Proteinuria
Pseudohypoparathyroidism and Albright Hereditary Osteodystrophy
Pulmonary Arterial Hypertension
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Radial Ray Abnormalities
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Renal Cystic Disease_SuperPanel
Renal Glomerular Disease_SuperPanel
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Retinal Disorders Superpanel
Retinitis pigmentosa
Rhabdomyolysis and Metabolic Myopathy
Sarcoma non-soft tissue
Sarcoma soft tissue
Schwannoma
Severe Combined Immunodeficiency
Severe early-onset obesity
Short QT syndrome
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Skeletal Dysplasia_Fetal
Skeletal Muscle Channelopathies
Speech apraxia
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Stickler Syndrome
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Susceptibility to Viral Infections
Syndromic Retinopathy
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
1.5025
Gene or Genomic Entity Name
ZFHX3_SCA4_GGC
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05 Jun 2026
Mendeliome v2.0
ZFHX3_SCA4_GGC
STR ZFHX3_SCA4_GGC: gene migrated from ENSG00000140836 to ENSG00000140836 (gene set migration)
27 Apr 2025
Mendeliome v1.2510
ZFHX3_SCA4_GGC
Bryony Thompson SCA4_ZFHX3_GGC was changed to ZFHX3_SCA4_GGC