TG, thyroglobulin, 7038

N. diseases: 240; N. variants: 43
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism
0.200 Biomarker disease RGD A novel missense mutation (G2320R) in thyroglobulin causes hypothyroidism in rdw rats. 11089535 2000
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism
0.200 Biomarker disease RGD [rdw rats, a new hereditary dwarf model in the rat]. 3366187 1988