TTF2, transcription termination factor 2, 8458

N. diseases: 19; N. variants: 0
Disease: Primary congenital hypothyroidism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3715197
Disease: Primary congenital hypothyroidism
Primary congenital hypothyroidism 		0.010 GeneticVariation disease BEFREE Therefore, in this study we investigated whether alanine (Ala) length polymorphisms and non-polymorphic mutations of the TTF-2 gene in pCH patients might be involved in the pathogenesis of pCH. 17318017 2007