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: C1848805
Disease: Thyroid Dyshormonogenesis 1
Thyroid Dyshormonogenesis 1
0.300 GermlineCausalMutation disease ORPHANET Genetic causes of congenital hypothyroidism due to dyshormonogenesis. 21543982 2011
CUI: C1848805
Disease: Thyroid Dyshormonogenesis 1
Thyroid Dyshormonogenesis 1
0.300 GermlineCausalMutation disease ORPHANET Congenital hypothyroidism. 20537182 2010