MeSH Browser

MeSH Supplementary: Thyroid Dyshormonogenesis 2A
Unique ID: C563206
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563206
Entry Term(s): Hypothyroidism, Congenital, due to Dyshormonogenesis, 2A; Iodide Peroxidase Deficiency; Thyroid Hormonogenesis, Genetic Defect in, 2A; Thyroid Peroxidase Deficiency
Registry Numbers: 0
Heading Mapped to: *Congenital Hypothyroidism; Iodide Peroxidase / deficiency
Frequency: 2
Note: mutation in Iodide Peroxidase
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Thyroid Dyshormonogenesis 2A MeSH Supplementary Concept Data 2025