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(HPO:0000851) | Congenital hypothyroidism | 16 / 7739 | ||||
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(OMIM) | Iodide organification defect | 1 / 7739 | ||||
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(OMIM) | Low T3 | 2 / 7739 | ||||
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(HPO:0000821) | Hypothyroidism | 141 / 7739 | ||||
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(OMIM) | Elevated TSH | 3 / 7739 | ||||
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(OMIM) | Increased RAI (radioactive iodine) uptake | 1 / 7739 | ||||
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(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 |