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Advanced Download Gene List
  • TNNI2
    • Sheldon-Hall Syndrome
  • SLC2A10
    • Hiatal Hernia
    • Arterial Tortuosity Syndrome
  • ABCC9
    • Cantú Syndrome
  • MYH3
    • Sheldon-Hall Syndrome
  • KCNJ8
    • Cantú Syndrome
  • LIPA
    • Acid Lipase Disease
  • KCNJ11
    • Diabetes Mellitus, Permanent Neonatal
  • TPM2
    • Sheldon-Hall Syndrome
  • CD55
    • Protein Losing Enteropathy
  • TNNT3
    • Sheldon-Hall Syndrome
  • PTEN
    • Intussusception
    • Social (Pragmatic) Communication Disorder
    • Thrombophlebitis
    • Protein Losing Enteropathy
  • RB1
    • Pinealoblastoma
    • Trilateral Retinoblastoma
  • MEN1
    • Gastrinoma
  • ABCC8
    • Diabetes Mellitus, Permanent Neonatal
  • GABRA5
    • Social (Pragmatic) Communication Disorder
  • SPG29
    • Spastic Paraplegia 29, Autosomal Dominant
  • COL1A1
    • Fibrous Dysplasia Of Bone
    • Hiatal Hernia
    • Hernia
  • THAS
    • Hernia
  • C9
    • Favre–racouchot Syndrome
  • PIEZO2
    • Sheldon-Hall Syndrome

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