TG, thyroglobulin, 7038

N. diseases: 240; N. variants: 43
Disease: Dwarfism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.410 Biomarker disease CTD_human A novel mutation in the thyroglobulin gene that causes goiter and dwarfism in Wistar Hannover GALAS rats. 24582622 2014
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.410 GeneticVariation disease BEFREE We have studied UPR development in two similar ERSDs, human congenital goiter caused by the C1264R and C1996S mutations in the thyroglobulin (Tg) gene and non-goitrous congenital hypothyroidism in rdw dwarf rats determined by the G2320R Tg mutation. 15171721 2004
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.410 Biomarker disease HPO