Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
0.500 Biomarker disease CTD_human Amiodarone-induced myxoedema coma. 24729111 2014
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
0.500 GermlineCausalMutation disease ORPHANET Clinical review: Central hypothyroidism: pathogenic, diagnostic, and therapeutic challenges. 22851492 2012
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
0.500 GermlineCausalMutation disease ORPHANET Congenital hypothyroidism. 20537182 2010
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
0.500 Biomarker disease CTD_human Induced hypothyroidism accelerates the regression of liver fibrosis in rats. 18031379 2007
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
0.500 GermlineCausalMutation disease ORPHANET Congenital secondary hypothyroidism due to a mutation C105Vfs114X thyrotropin-beta mutation: genetic study of five unrelated families from Switzerland and Argentina. 12930599 2003