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  • OPN1LW
    • Colorblindness, Partial, Protan Series
    • Color Blindness
    • Color Vision Deficiency
  • OPN1MW
    • Colorblindness, Partial, Deutan Series
    • Color Vision Deficiency
  • ABHD5
    • Cerebral Creatine Deficiency
  • MYO5B
    • Microvillus Inclusion Disease
  • ATRX
    • Alpha-Thalassemia Mental Retardation Syndrome
  • GAMT
    • Guanidinoacetate Methyltransferase Deficiency
  • BEST1
    • Vitelliform Macular Dystrophy
  • MED12
    • Fg Syndrome
    • Alpha-Thalassemia Mental Retardation Syndrome
  • ALS2
    • Infantile-Onset Ascending Hereditary Spastic Paralysis
  • UBA1
    • X-Linked Spinal Muscular Atrophy Type 2
  • MC2R
    • Familial Glucocorticoid Deficiency
  • NR2E3
    • Color Vision Deficiency
    • Goldmann-Favre Syndrome
  • BLVRA
    • Hyperbiliverdinemia
  • OFD1
    • Orofaciodigital Syndrome 1
  • STX3
    • Microvillus Inclusion Disease
  • SRD5A2
    • Alopecia, Androgenetic, 1
  • AR
    • Alopecia, Androgenetic, 1
    • Colorblindness, Partial, Protan Series
  • TMEM107
    • Orofaciodigital Syndrome 1
  • CNGA3
    • Color Blindness
    • Color Vision Deficiency
  • PRPH2
    • Vitelliform Macular Dystrophy

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