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Thyroid Dyshormonogenesis 6 [Supplementary Concept]

mutation in DUOX2

Date introduced: November 5, 2012

MeSH Unique ID: C564608

Heading Mapped to:

Entry Terms:

  • Thyroid Hormonogenesis, Genetic Defect in, 6
  • Hypothyroidism, Congenital, due to Dyshormonogenesis, 6

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