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  • CEP290
    • Meckel Syndrome, Type 11
    • Retinitis Pigmentosa 57
    • Joubert Syndrome 16
  • MYO5B
    • Microvillus Inclusion Disease
    • Fanconi Renotubular Syndrome 2
  • RPGRIP1
    • Meckel Syndrome, Type 11
    • Retinitis Pigmentosa 57
  • C8orf37
    • Retinitis Pigmentosa 57
  • TMEM231
    • Meckel Syndrome, Type 11
    • Joubert Syndrome 16
  • PDE6B
    • Retinitis Pigmentosa 57
  • PDE6A
    • Retinitis Pigmentosa 57
  • CRX
    • Pinealoblastoma
    • Retinitis Pigmentosa 57
  • RPGR
    • Retinitis Pigmentosa 57
  • RPE65
    • Retinitis Pigmentosa 57
  • VSX2
    • Retinitis Pigmentosa 57
    • Microphthalmia, Isolated 2
  • ALS2
    • Infantile-Onset Ascending Hereditary Spastic Paralysis
  • LPIN2
    • Majeed Syndrome
  • CC2D2A
    • Meckel Syndrome, Type 11
    • Retinitis Pigmentosa 57
    • Joubert Syndrome 16
  • PDE6G
    • Retinitis Pigmentosa 57
  • LRAT
    • Retinitis Pigmentosa 57
  • TAF2
    • Mental Retardation, Autosomal Recessive 40
  • MC2R
    • Familial Glucocorticoid Deficiency
  • KANK2
    • Palmoplantar Keratoderma And Woolly Hair
  • CEP19
    • Morbid Obesity And Spermatogenic Failure

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