| familiaire hyperthyreoïdie door mutatie in thyrotropinereceptor (aandoening) | | familiaire hyperthyreoïdie door mutatie in thyrotropinereceptor | | familiaire hyperthyroïdie door mutatie in TSH-receptor
familiaire niet-immune hyperthyroïdie
| | 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. |
| | Id | 716743006 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E05.8 | | Term | Overige gespecificeerde vormen van thyrotoxicose |
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| SNOMED CT to Orphanet simple map | 424 |
| SNOMED CT to ICD-10 extended map | | Target | E05.8 | | Rule | TRUE | | Advice | ALWAYS E05.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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