Hyperthyreose durch TSH-Rezeptor-Genmutationen, familiäre Form
ORPHA:424· ICD-10 E05.8· Familial hyperthyroidism due to mutations in TSH receptor
- Prävalenz
- Unknown
- Vererbung
- Autosomal dominant
- Erkrankungsalter
- All ages
ORPHA:424· ICD-10 E05.8· Familial hyperthyroidism due to mutations in TSH receptor