Hereditary hyperthyroidism due to mutations in TSH receptor (Q86377): Difference between revisions
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Revision as of 11:46, 15 August 2026
Familial hyperthyroidism due to mutations in thyroid stimulating hormone (TSH) receptor is a hereditary non-autoimmune hyperthyroidism. It is characterised by the presence of signs and symptoms of hyperthyroidism and diffuse goitre without evidence of an autoimmune aetiology.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_727171381 |
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| English | Hereditary hyperthyroidism due to mutations in TSH receptor |
Familial hyperthyroidism due to mutations in thyroid stimulating hormone (TSH) receptor is a hereditary non-autoimmune hyperthyroidism. It is characterised by the presence of signs and symptoms of hyperthyroidism and diffuse goitre without evidence of an autoimmune aetiology. |
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CID11:ID_727171381
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dki-india-ID_727171381
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