• FindZebra
  • About
  • Contact
  • Help
  • Login
Advanced Download Gene List
  • TTPA
    • Familial Isolated Vitamin E Deficiency
  • SLC6A19
    • Hartnup Disease
  • FMR1
    • Renpenning's Syndrome
    • Fg Syndrome
    • Fragile X-Associated Tremor/ataxia Syndrome
  • TMC6
    • Epidermodysplasia Verruciformis
  • SLC12A6
    • Andermann Syndrome
  • PQBP1
    • Renpenning's Syndrome
  • MED12
    • Fg Syndrome
  • TAF1
    • Dystonia 3, Torsion, X-Linked
  • GNAQ
    • Sturge–weber Syndrome
  • FAM20A
    • Enamel-Renal Syndrome
  • NGLY1
    • Ngly1 Deficiency
  • UBE3B
    • Kaufman Oculocerebrofacial Syndrome
  • RHBDF2
    • Howel–evans Syndrome
  • IFIH1
    • Singleton Merten Syndrome
  • TMC8
    • Epidermodysplasia Verruciformis
  • ACTG2
    • Berdon Syndrome
  • FLNA
    • Intestinal Neuronal Dysplasia
    • Fg Syndrome
  • RASA1
    • Sturge–weber Syndrome
  • ASS1
    • Citrullinemia Type I
  • MYH11
    • Berdon Syndrome

FindZebra

contact@findzebra.com