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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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Angelman Rett like syndromes
Anophthalmia_Microphthalmia_Coloboma
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Arrhythmia_SuperPanel
Arrhythmogenic Cardiomyopathy
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Ataxia
Atrial Fibrillation
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Autism
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Cardiomyopathy_Adult_SuperPanel
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Deafness_IsolatedAndComplex
Defects of intrinsic and innate immunity
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Diamond Blackfan anaemia
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Ectodermal Dysplasia
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Epidermolysis bullosa
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Genomic newborn screening: BabyScreen+
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Glaucoma congenital
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Hair 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
Long QT Syndrome
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Mackenzie's Mission_Reproductive Carrier Screening
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Malignant Hyperthermia Susceptibility
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Movement Disorders Superpanel
Multiple pterygium syndrome_Fetal akinesia sequence
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Myopathy Superpanel
Neuroblastoma
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Neuromuscular Superpanel
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Palmoplantar Keratoderma and Erythrokeratoderma
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Periventricular Grey Matter Heterotopia
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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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Radial Ray Abnormalities
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Renal Cystic Disease_SuperPanel
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Repeat Disorders
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
Spontaneous coronary artery dissection
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
0.272
Gene or Genomic Entity Name
FOXL2_BPES_GCN
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14 Apr 2026
Repeat Disorders v1.0
FOXL2_BPES_GCN
STR FOXL2_BPES_GCN: gene migrated from ENSG00000183770 to ENSG00000183770 (gene set migration)
24 Apr 2025
Repeat Disorders v0.169
FOXL2_BPES_GCN
Bryony Thompson BPES was changed to FOXL2_BPES_GCN