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