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Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic
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Motor Neurone Disease
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Multiple joint dislocations and laxity
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Multiple pterygium syndrome_Fetal akinesia sequence
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Muscular dystrophy and myopathy_Paediatric
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NCGC
NCGC
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Pain syndromes
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Palmoplantar Keratoderma and Erythrokeratoderma
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Periventricular Grey Matter Heterotopia
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Pharmacogenomics_Paediatric
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Pierre Robin Sequence
Pierre Robin Sequence
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Prepair 1000+
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Prepair 500+
Prepair 500+
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Primary Ovarian Insufficiency_Premature Ovarian Failure
Progressive Myoclonic Epilepsy
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Progressive Neurological Conditions
Proteinuria
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Pseudohypoparathyroidism and Albright Hereditary Osteodystrophy
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Retinitis Pigmentosa Superpanel
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Rhabdomyolysis and Metabolic Myopathy
Sarcoma
Sarcoma
Schwannomatosis
Schwannomatosis
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Severe Combined Immunodeficiency (absent T present B cells)
Severe Combined Immunodeficiency (absent T absent B cells)
Severe Combined Immunodeficiency (absent T absent B cells)
Severe early-onset obesity
Severe early-onset obesity
Short Long Bones with Advanced Carpal Bone Age
Short Long Bones with Advanced Carpal Bone Age
Short QT syndrome
Short QT syndrome
Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy
Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy
Sick sinus syndrome
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Stickler Syndrome
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Stroke
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Syndromic Retinopathy
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TCGA_PANCAN_2018
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Transplant Co-Morbidity Superpanel
Transplant Co-Morbidity Superpanel
Tremors_Superpanel
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly
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2.0
Gene or Genomic Entity Name
DPM3
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05 Feb 2026
Limb-Girdle Muscular Dystrophy and Distal Myopathy v2.0
DPM3
Gene migrated from ENSG00000179085 to ENSG00000179085 (gene set migration)