Myotonia congenita (Q587420)

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Human disease
  • Congenital myotonia, NOS
  • Congenital myotonia, autosomal dominant form (disorder)
  • Thomsen's disease
  • myotonia congenita
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Language Label Description Also known as
English
Myotonia congenita
Human disease
  • Congenital myotonia, NOS
  • Congenital myotonia, autosomal dominant form (disorder)
  • Thomsen's disease
  • myotonia congenita

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