Congenital hypothyroidism due to thyroid peroxidase mutations (Q92193): Difference between revisions
From determinar.ia.br - Determine suas informações
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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. Este diagnóstico é devido a mutações na peroxidase tireoidiana. | |||
| 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 thyroid peroxidase mutations. | |||
Revision as of 07:20, 16 August 2026
This is a congenital state in which the thyroid gland does not make enough thyroid hormone. This diagnosis is due to thyroid peroxidase mutations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_179437280 |
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| English | Congenital hypothyroidism due to thyroid peroxidase mutations |
This is a congenital state in which the thyroid gland does not make enough thyroid hormone. This diagnosis is due to thyroid peroxidase mutations. |
