Transient congenital hypothyroidism due to monoallelic or biallelic mutations of dual oxidase 2 mutation (Q86208): Difference between revisions
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Latest revision as of 11:34, 15 August 2026
This is a transient congenital state in which the thyroid gland does not make enough thyroid hormone. This diagnosis is due to heterozygous mutations of monoallelic or biallelic mutations of dual oxidase 2 mutation [DUOX2]
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1830092908 |
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| English | Transient congenital hypothyroidism due to monoallelic or biallelic mutations of dual oxidase 2 mutation |
This is a transient congenital state in which the thyroid gland does not make enough thyroid hormone. This diagnosis is due to heterozygous mutations of monoallelic or biallelic mutations of dual oxidase 2 mutation [DUOX2] |
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CID11:ID_1830092908
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dki-india-ID_1830092908
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Concluído
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13 August 2026
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