TPO

thyroid peroxidase
OMIM: 606765
PanelMode of inheritanceDetails
1 panel
R-numbers: R145
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Congenital hypothyroidism, Thyroid dyshormonogenesis 2A, 274500, TDH2A, Iodide organification defect, goitre