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: C0302859
Disease: Euthyroid Goiter
Euthyroid Goiter
0.070 GeneticVariation disease BEFREE Up to now, 62 inactivating mutations in the TG gene have been identified in patients with congenital goiter and endemic or non-endemic simple goiter. 23164529 2013
CUI: C0302859
Disease: Euthyroid Goiter
Euthyroid Goiter
0.070 GeneticVariation disease BEFREE Mutations in TG gene have been also reported associated with endemic and euthyroid nonendemic simple goiter. 20093166 2010
CUI: C0302859
Disease: Euthyroid Goiter
Euthyroid Goiter
0.070 GeneticVariation disease BEFREE Mutations in the human thyroglobulin gene are associated with congenital goiter or endemic and nonendemic simple goiter. 16870170 2006
CUI: C0302859
Disease: Euthyroid Goiter
Euthyroid Goiter
0.070 GeneticVariation disease BEFREE This result suggests that Tg mutations may provide a genetic basis for the cause of familial euthyroid goiter. 16720658 2006
CUI: C0302859
Disease: Euthyroid Goiter
Euthyroid Goiter
0.070 AlteredExpression disease BEFREE We compared three methods of blood collection and RNA extraction, and quantified Tg mRNA (by real time RT-PCR) in the peripheral blood of a) probands without thyroid disease (n=42), patients with b) thyroid autonomy (n=15), c) Graves' disease (n=22), d) euthyroid goiter (n=6), and in DTC-patients after thyroidectomy and radioiodine therapy e) with (n=16) and f) without (n=37) metastasis. 12444888 2002
CUI: C0302859
Disease: Euthyroid Goiter
Euthyroid Goiter
0.070 GeneticVariation disease BEFREE We have previously demonstrated that some cases of endemic and nonendemic simple goiter are associated with a mutation within exon 10 of the thyroglobulin gene. 11525274 2001
CUI: C0302859
Disease: Euthyroid Goiter
Euthyroid Goiter
0.070 GeneticVariation disease BEFREE To our knowledge, this is the first time that a mutation in the thyroglobulin gene has been described in a patient with endemic simple goiter and further confirms the association between the exon 10 mutation and development of goiter. 8936666 1996