thyroid dyshormonogenesis 3

Summary
Synonym
  • TDH3
  • genetic defect in thyroid hormonogenesis 3
Definition
A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TG on chromosome 8q24.22.
Super Class
autosomal recessive disease familial thyroid dyshormonogenesis
Disease Ontology
DOID:0112187
Mondo Disease Ontology
MeSH
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7038 TG thyroglobulin
Displaying 1 entry
Gene ID Gene Symbol Description Source
21819 Tg thyroglobulin

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024