Thyroid Dyshormonogenesis 2A [Supplementary Concept]
mutation in Iodide Peroxidase
Date introduced: November 5, 2012
MeSH Unique ID: C563206
Heading Mapped to:
Entry Terms:
- Thyroid Hormonogenesis, Genetic Defect in, 2A
- Hypothyroidism, Congenital, due to Dyshormonogenesis, 2A
- Iodide Peroxidase Deficiency
- Thyroid Peroxidase Deficiency