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Thyroid Dyshormonogenesis 1 MeSH Supplementary Concept Data 2024


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
Registry Number
0
Heading Mapped to
*Congenital Hypothyroidism
Frequency
3
Note
mutation in SLC5A5
Date of Entry
2012/11/05
Thyroid Dyshormonogenesis 1 Preferred
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