MeSH Browser

MeSH Supplementary: Thyroid Dyshormonogenesis 1
Unique ID: C564766
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564766
Entry Term(s): Hypothyroidism, Congenital, due to Dyshormonogenesis, 1; Iodine Accumulation, Transport, or Trapping Defect; Thyroid Hormonogenesis, Genetic Defect in, 1
Heading Mapped to: *Congenital Hypothyroidism
Frequency: 3
Note: mutation in SLC5A5
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Thyroid Dyshormonogenesis 1 MeSH Supplementary Concept Data 2024