Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder) | | Familial non-autoimmune autosomal dominant hyperthyroidism | | Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor Familial non-immune hyperthyroidism
| | A rare hyperthyroidism characterized by mild to severe hyperthyroidism, presence of goiter, absence of features of autoimmunity, frequent relapses while on treatment and a positive family history. | | familiaire hyperthyreoïdie door mutatie in thyrotropinereceptor | | familiaire hyperthyroïdie door mutatie in TSH-receptor familiaire niet-immune hyperthyroïdie
|
| Id | 716743006 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | E05.8 | Rule | TRUE | Advice | ALWAYS E05.8 | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|