TPO, thyroid peroxidase, 7173

N. diseases: 306; N. variants: 47
Disease: Myxedema, Congenital ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1578691
Disease: Myxedema, Congenital
Myxedema, Congenital 		0.300 Biomarker disease CTD_human Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis. 17381485 2007
CUI: C1578691
Disease: Myxedema, Congenital
Myxedema, Congenital 		0.300 Biomarker disease CTD_human Total iodide organification defect: clinical and molecular characterization of an Italian family. 16187919 2005
CUI: C1578691
Disease: Myxedema, Congenital
Myxedema, Congenital 		0.300 Biomarker disease CTD_human Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect. 14751036 2003
CUI: C1578691
Disease: Myxedema, Congenital
Myxedema, Congenital 		0.300 Biomarker disease CTD_human Congenital hypothyroidism with goiter in toy fox terriers. 12564727 2003