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  • LMNA
    • Muscular Dystrophy, Pseudohypertrophic, With Internalized Capillaries
    • Limb-Girdle Muscular Dystrophy
    • Muscular Dystrophy, Scapulohumeral
    • Congenital Fiber-Type Disproportion
    • Minicore Myopathy With External Ophthalmoplegia
  • ACTA1
    • Limb-Girdle Muscular Dystrophy
    • Congenital Fiber-Type Disproportion
    • Nemaline Myopathy 1
  • DMD
    • Muscular Dystrophy, Pseudohypertrophic, With Internalized Capillaries
    • Limb-Girdle Muscular Dystrophy
    • Muscular Dystrophy, Scapulohumeral
  • ASL
    • Argininosuccinic Aciduria
  • FKRP
    • Muscular Dystrophy, Pseudohypertrophic, With Internalized Capillaries
    • Limb-Girdle Muscular Dystrophy
    • Congenital Fiber-Type Disproportion
    • Holoprosencephaly
    • Minicore Myopathy With External Ophthalmoplegia
  • TPM3
    • Congenital Fiber-Type Disproportion
    • Nemaline Myopathy 1
  • TTPA
    • Familial Isolated Vitamin E Deficiency
  • SGCE
    • Myoclonic Dystonia
  • SCN9A
    • Small Fiber Peripheral Neuropathy
    • Small Fiber Neuropathy
  • PMM2
    • Pmm2 Deficiency
  • TPM2
    • Congenital Fiber-Type Disproportion
    • Nemaline Myopathy 1
  • POMT1
    • Limb-Girdle Muscular Dystrophy
    • Congenital Fiber-Type Disproportion
    • Holoprosencephaly
    • Minicore Myopathy With External Ophthalmoplegia
  • PABPN1
    • Oculopharyngeal Muscular Dystrophy
  • FKTN
    • Limb-Girdle Muscular Dystrophy
    • Congenital Fiber-Type Disproportion
    • Holoprosencephaly
    • Minicore Myopathy With External Ophthalmoplegia
  • POMGNT1
    • Limb-Girdle Muscular Dystrophy
    • Congenital Fiber-Type Disproportion
    • Holoprosencephaly
    • Minicore Myopathy With External Ophthalmoplegia
  • SELENON
    • Congenital Fiber-Type Disproportion
    • Minicore Myopathy With External Ophthalmoplegia
  • PQBP1
    • Renpenning's Syndrome
  • GALE
    • Galactose Epimerase Deficiency
  • LARGE1
    • Muscular Dystrophy, Pseudohypertrophic, With Internalized Capillaries
    • Muscular Dystrophy, Scapulohumeral
    • Congenital Fiber-Type Disproportion
    • Holoprosencephaly
    • Minicore Myopathy With External Ophthalmoplegia
  • ITGA7
    • Congenital Fiber-Type Disproportion
    • Minicore Myopathy With External Ophthalmoplegia

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