Congenital hypothyroidism due to iodine or sodium symporter mutations (Q92170): Difference between revisions
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
Este é um estado congênito em que a glândula tireoide não produz hormônio tireoidiano suficiente. O diagnóstico é devido a mutações no simportador de iodo/sódio. | |||
| description / en | description / en | ||
This is a congenital state in which the thyroid gland does not make enough thyroid hormone. This diagnosis is due to iodine/sodium symporter mutations. | |||
Revision as of 07:19, 16 August 2026
This is a congenital state in which the thyroid gland does not make enough thyroid hormone. This diagnosis is due to iodine/sodium symporter mutations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_51038683 |
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| English | Congenital hypothyroidism due to iodine or sodium symporter mutations |
This is a congenital state in which the thyroid gland does not make enough thyroid hormone. This diagnosis is due to iodine/sodium symporter mutations. |
