Hypotyreóza způsobená mutací TSH receptoru
ORPHA:90673· ICD-10 E03.1· Hypothyroidism due to TSH receptor mutations
- Prevalence
- Unknown
- Dědičnost
- Autosomal dominant, Autosomal recessive
- Věk nástupu
- Infancy, Neonatal
ORPHA:90673· ICD-10 E03.1· Hypothyroidism due to TSH receptor mutations