Hypothyreose, kongenitale, durch heterozygote THOX2-Genmutationen
ORPHA:226316· ICD-10 P72.2· Genetic transient congenital hypothyroidism
- Vererbung
- Autosomal recessive
- Erkrankungsalter
- Infancy, Neonatal
ORPHA:226316· ICD-10 P72.2· Genetic transient congenital hypothyroidism