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Deep Research Advanced Download Gene List
  • PROM1
    • Stargardt Disease 4
    • Cone-Rod Dystrophy 12
    • Cone-Rod Dystrophy 11
    • Macular Dystrophy, Retinal, 2
  • MAGEL2
    • Schaaf-Yang Syndrome
    • Schaaf-Yang Syndrome
    • Kyphosis
  • ABCA4
    • Stargardt Disease 4
    • Cone-Rod Dystrophy 11
  • ABHD5
    • Cerebral Creatine Deficiency
  • ATRX
    • Alpha-Thalassemia Mental Retardation Syndrome
  • SNAP29
    • Cerebral Dysgenesis–neuropathy–ichthyosis–keratoderma Syndrome
  • SLC40A1
    • Hemochromatosis Type 4
  • GAMT
    • Guanidinoacetate Methyltransferase Deficiency
  • FMR1
    • Renpenning's Syndrome
    • Fragile X-Associated Tremor/ataxia Syndrome
    • Schaaf-Yang Syndrome
  • PMM2
    • Pmm2 Deficiency
    • Kyphosis
  • PQBP1
    • Renpenning's Syndrome
  • SNRPN
    • Cone-Rod Dystrophy 11
    • Schaaf-Yang Syndrome
    • Kyphosis
  • CEACAM16
    • Deafness, Autosomal Dominant 4a
    • Deafness, Autosomal Dominant 4b
  • CRX
    • Pinealoblastoma
    • Stargardt Disease 4
    • Cone-Rod Dystrophy 11
  • SLC2A1
    • Glucose Transporter Type 1 Deficiency Syndrome
  • PDGFRB
    • Cerebral Creatine Deficiency
    • Primary Familial Brain Calcification
    • Chordoma, Susceptibility To
  • SLC20A2
    • Primary Familial Brain Calcification
  • GALE
    • Galactose Epimerase Deficiency
  • COL18A1
    • Knobloch Syndrome 1
  • DSG1
    • Palmoplantar Keratoderma I, Striate, Focal, Or Diffuse

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