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Achromatopsia
Additional findings_Adult
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Adrenal insufficiency
Adult Cardiac SuperPanel
Alagille syndrome
Alternating Hemiplegia and Hemiplegic Migraine
Amelogenesis imperfecta
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Arrhythmia_SuperPanel
Arrhythmogenic Cardiomyopathy
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Atrial Fibrillation
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Basal Cell Cancer
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Cataract
Catecholaminergic Polymorphic Ventricular Tachycardia
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Choanal atresia
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Chromosome Breakage Disorders
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Colorectal Cancer and Polyposis
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Cone-rod Dystrophy
Congenital adrenal hyperplasia
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Congenital diaphragmatic hernia
Congenital Diarrhoea
Congenital Disorders of Glycosylation
Congenital Heart Defect
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Corneal Dystrophy
Craniosynostosis
Cutis Laxa
Deafness_IsolatedAndComplex
Defects of intrinsic and innate immunity
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Diabetes Insipidus
Diamond Blackfan anaemia
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Diffuse Gastric Cancer
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Disorders of immune dysregulation
Dyslipidaemia
Dystonia and Chorea
Early-onset Dementia
Early-onset Parkinson disease
Ectodermal Dysplasia
Endometrial Cancer
Epidermolysis bullosa
Eye Anterior Segment Abnormalities
Facial papules
Familial hypercholesterolaemia
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Foveal Hypoplasia
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Genomic newborn screening: BabyScreen+
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Glaucoma congenital
Glycogen Storage Diseases
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Haematuria_Alport
Haem degradation and bilirubin metabolism defects
Hair disorders
Hand and foot malformations
Hereditary angioedema
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Hereditary Neuropathy
Hereditary Pigmentary Disorders
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IBMDx study
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Immune_markers_WTS_UMCCR
Immunological disorders_SuperPanel
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Incidentalome
Incidentalome_PREGEN_DRAFT
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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
Long QT Syndrome
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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
Neuroblastoma
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Palmoplantar Keratoderma and Erythrokeratoderma
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Pharmacogenomics_Paediatric
Photosensitivity Syndromes
Pierre Robin Sequence
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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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Renal Cystic Disease_SuperPanel
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Retinal Disorders Superpanel
Retinitis pigmentosa
Rhabdomyolysis and Metabolic Myopathy
Sarcoma non-soft tissue
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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
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1.0
0.543
Gene or Genomic Entity Name
ODAD4
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07 Jun 2026
Congenital Heart Defect v1.0
ODAD4
Gene symbol changed from TTC25 to ODAD4 during gene set migration (ENSG00000204815 -> ENSG00000204815)