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Advanced Download Gene List
  • ASL
    • Argininosuccinic Aciduria
  • TBX5
    • Holt–oram Syndrome
  • PMM2
    • Pmm2 Deficiency
  • SLC6A19
    • Hartnup Disease
  • TNF
    • Acute Promyelocytic Leukemia
    • Asystole
    • Ophthalmia
    • Familial Isolated Vitamin E Deficiency
    • Renpenning's Syndrome
    • Tetraplegia
  • PYGM
    • Glycogen Storage Disease Type V
  • TTPA
    • Familial Isolated Vitamin E Deficiency
  • SGCE
    • Myoclonic Dystonia
  • IFNG
    • Acute Promyelocytic Leukemia
    • Asystole
    • Ophthalmia
    • Vascular Tumor
  • PRPS1
    • Arts Syndrome
    • Tetraplegia
  • PQBP1
    • Renpenning's Syndrome
  • LIPA
    • Acid Lipase Disease
    • Asystole
  • IFIH1
    • Singleton Merten Syndrome
  • NPM1
    • Acute Promyelocytic Leukemia
  • RARA
    • Acute Promyelocytic Leukemia
  • TRNL1
    • Merrf Syndrome
  • VEGFA
    • Corneal Neovascularization
    • Acute Promyelocytic Leukemia
    • Asystole
    • Ophthalmia
    • Primary Peritoneal Carcinoma
    • Vascular Malformation
  • IL1B
    • Corneal Neovascularization
    • Merrf Syndrome
    • Acute Promyelocytic Leukemia
    • Asystole
    • Ophthalmia
    • Renpenning's Syndrome
  • ITGB2
    • Acute Promyelocytic Leukemia
    • Leukocyte Adhesion Deficiency, Type I
  • NUMA1
    • Acute Promyelocytic Leukemia

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