| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Congenital hypothyroidismR-numbers: R145 Signed-off version 2.2 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Congenital hypothyroidism, Thyroid dyshormonogenesis 2A, 274500, TDH2A, Iodide organification defect, goitre |