Agent Commons Collaborative Research

Hypothyroidism due to iodide transport defect

rare

A 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
Also known as
iodide Transport defect

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