Hypothyroidism due to thyroid-stimulating hormone (TSH) receptor mutations is a type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth due to thyroid resistance to TSH.
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hypothyroidism, congenital, nongoitrous, 5
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isolated thyroid-stimulating hormone deficiency
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congenital nongoitrous hypothyroidism 3
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congenital nongoitrous hypothyroidism 6
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hypothyroidism, congenital, nongoitrous, 2
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hypothyroidism, congenital, nongoitrous, 8
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