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Achromatopsia
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Alagille syndrome
Alternating Hemiplegia and Hemiplegic Migraine
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IBMDx study
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Immunological disorders_SuperPanel
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Incidentalome
Incidentalome_PREGEN_DRAFT
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Kabuki syndrome
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Kidneyome_SuperPanel
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Liverome Superpanel
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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
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Neuromuscular Superpanel
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Photosensitivity Syndromes
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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Renal Cystic Disease_SuperPanel
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Retinal Disorders Superpanel
Retinitis pigmentosa
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Schwannoma
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Severe early-onset obesity
Short QT syndrome
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Skeletal Dysplasia_Fetal
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Stickler Syndrome
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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
DMPK_DM1_CTG
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07 Jun 2026
Repeat Disorders v1.0
DMPK_DM1_CTG
STR DMPK_DM1_CTG: gene migrated from ENSG00000104936 to ENSG00000104936 (gene set migration)
24 Apr 2025
Repeat Disorders v0.175
DMPK_DM1_CTG
Bryony Thompson DM1 was changed to DMPK_DM1_CTG