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Advanced Download Gene List
  • ASL
    • Argininosuccinic Aciduria
  • PMM2
    • Pmm2 Deficiency
    • Hypertelorism
  • TBX5
    • Holt-Oram Syndrome
  • PEX1
    • Peroxisome Biogenesis Disorder 10a (Zellweger)
    • Hypertelorism
  • MED13L
    • Congenitally Uncorrected Transposition Of The Great Arteries
    • Hypertelorism
  • FOXE3
    • Aortic Aneurysm, Familial Thoracic 11, Susceptibility To
    • Hypertelorism
  • GATA2
    • Immunodeficiency 21
  • GALK1
    • Galactokinase Deficiency
  • FOXP2
    • Foxp2-Related Speech And Language Disorder
  • ADGRG1
    • Bilateral Frontoparietal Polymicrogyria
  • FOXG1
    • Foxg1 Syndrome
  • TBX19
    • Acth Deficiency, Isolated
  • FBXO7
    • Parkinson Disease 15, Autosomal Recessive Early-Onset
  • FBXL4
    • Mitochondrial Dna Depletion Syndrome 13 (Encephalomyopathic Type)
  • PEX3
    • Peroxisome Biogenesis Disorder 10a (Zellweger)
    • Hypertelorism
  • PEX6
    • Peroxisome Biogenesis Disorder 10a (Zellweger)
    • Hypertelorism
  • PEX2
    • Peroxisome Biogenesis Disorder 10a (Zellweger)
    • Hypertelorism
  • COX4I2
    • Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
  • PEX26
    • Peroxisome Biogenesis Disorder 10a (Zellweger)
    • Hypertelorism
  • CFH
    • Membranoproliferative Glomerulonephritis

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