Hereditary hyperthyroidism due to mutations in TSH receptor (Q86377): Difference between revisions
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Hipertireoidismo familiar devido a mutações no receptor do hormônio tireoestimulante (TSH) é um hipertireoidismo hereditário não autoimune. É caracterizado pela presença de sinais e sintomas de hipertireoidismo e de bócio difuso sem evidências de etiologia autoimune. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
