Transient congenital hypothyroidism due to heterozygous mutations of THOX2 (Q86205)
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Defects in the thyroid oxidase 2 (THOX2) gene result in a lack of H2O2, which is a protein essential for thyroid hormone synthesis. Therefore, heterozygous mutations in this gene lead to transient congenital hypothyroidism.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1663592623 |
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| English | Transient congenital hypothyroidism due to heterozygous mutations of THOX2 |
Defects in the thyroid oxidase 2 (THOX2) gene result in a lack of H2O2, which is a protein essential for thyroid hormone synthesis. Therefore, heterozygous mutations in this gene lead to transient congenital hypothyroidism. |
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CID11:ID_1663592623
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dki-india-ID_1663592623
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Concluído
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13 August 2026
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