Transient congenital hypothyroidism due to monoallelic or biallelic mutations of dual oxidase 2 mutation (Q86208): Difference between revisions
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Se refere a um estado congênito transitório em que a glândula tireoide não produz hormônios tireoidianos suficiente. Este diagnóstico é devido a mutações heterozigóticas de mutações monoalélicas ou bialélicas da mutação dual de oxidase 2 (DUOX2). | |||
| description / en | description / en | ||
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] | |||
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] |
