Thyroid Dyshormonogenesis 2A [Supplementary Concept]

mutation in Iodide Peroxidase

Date introduced: November 5, 2012

MeSH Unique ID: C563206

Heading Mapped to:

• Congenital Hypothyroidism
• Iodide Peroxidase/deficiency

Entry Terms:

• Thyroid Hormonogenesis, Genetic Defect in, 2A
• Hypothyroidism, Congenital, due to Dyshormonogenesis, 2A
• Iodide Peroxidase Deficiency
• Thyroid Peroxidase Deficiency