Hereditary hyperthyroidism due to mutations in TSH receptor (Q86377): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-ID_727171381 | |||
| Property / Canary Token: dki-india-ID_727171381 / rank | |||
Normal rank | |||
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 |
||
| 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. |
Statements
CID11:ID_727171381
0 references
dki-india-ID_727171381
0 references
