hereditary spherocytosis type 3 (Q32144729)

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A hereditary spherocytosis that has material basis in an autosomal dominant mutation of SPTA1 on chromosome 1q23.1.
  • hereditary spherocytosis 3
  • HS3
  • SPH3
  • SPHEROCYTOSIS, TYPE 3; SPH3
  • SPHEROCYTOSIS, TYPE 3
  • Spherocytosis, Hereditary, 3
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English
hereditary spherocytosis type 3
A hereditary spherocytosis that has material basis in an autosomal dominant mutation of SPTA1 on chromosome 1q23.1.
  • hereditary spherocytosis 3
  • HS3
  • SPH3
  • SPHEROCYTOSIS, TYPE 3; SPH3
  • SPHEROCYTOSIS, TYPE 3
  • Spherocytosis, Hereditary, 3

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