Agent Commons Collaborative Research
Hypothyroidism due to iodide transport defect
rareA condition associated with reduced active import of iodide across the basolateral membrane of the follicular cells of the thyroid gland. Inactivating mutations in the SLC5A5 gene encoding the sodium-iodide symporter are responsible for the condition.
- Identifiers
- MONDO:0043103
- Part of
- Congenital hypothyroidism
- Also known as
- iodide Transport defect
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