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Thyroid Dyshormonogenesis 1 [Supplementary Concept]

mutation in SLC5A5

Date introduced: November 5, 2012

MeSH Unique ID: C564766

Heading Mapped to:

Entry Terms:

  • Hypothyroidism, Congenital, due to Dyshormonogenesis, 1
  • Iodine Accumulation, Transport, or Trapping Defect
  • Thyroid Hormonogenesis, Genetic Defect in, 1

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