Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1848794
Disease: Thyrotropin, Biologically Inactive
Thyrotropin, Biologically Inactive
0.300 GermlineCausalMutation phenotype ORPHANET Clinical review: Central hypothyroidism: pathogenic, diagnostic, and therapeutic challenges. 22851492 2012
CUI: C1848794
Disease: Thyrotropin, Biologically Inactive
Thyrotropin, Biologically Inactive
0.300 GermlineCausalMutation phenotype ORPHANET Congenital hypothyroidism. 20537182 2010
CUI: C1848794
Disease: Thyrotropin, Biologically Inactive
Thyrotropin, Biologically Inactive
0.300 GermlineCausalMutation phenotype ORPHANET Congenital secondary hypothyroidism due to a mutation C105Vfs114X thyrotropin-beta mutation: genetic study of five unrelated families from Switzerland and Argentina. 12930599 2003