Hereditary hyperthyroidism due to mutations in TSH receptor (Q86377): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed label, description and/or aliases in pt-br, en
‎Changed an Item
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/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