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Achromatopsia
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Alagille syndrome
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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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Lipodystrophy_Lipoatrophy
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Liverome Superpanel
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Mackenzie's Mission_Reproductive Carrier Screening
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Myopathy Superpanel
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Pharmacogenomics_Paediatric
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Pierre Robin Sequence
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Prepair 1000+
Prepair 500+
Primary nodular adrenocortical disease
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Prostate Cancer
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Pulmonary Arterial Hypertension
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Renal Cystic Disease_SuperPanel
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Retinal Disorders Superpanel
Retinitis pigmentosa
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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
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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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2.0
1.5025
Gene or Genomic Entity Name
ARSL
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05 Jun 2026
Mendeliome v2.0
ARSL
Gene symbol changed from ARSE to ARSL during gene set migration (ENSG00000157399 -> ENSG00000157399)