TAT, tyrosine aminotransferase, 6898

N. diseases: 230; N. variants: 28
Disease: Tyrosinemias ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268483
Disease: Tyrosinemias
Tyrosinemias 		0.420 GeneticVariation disease BEFREE To this end, we sought TAT gene mutations in 9 tyrosinaemia II patients from three consanguineous Palestinian kindreds. 16917729 2006
CUI: C0268483
Disease: Tyrosinemias
Tyrosinemias 		0.420 AlteredExpression disease BEFREE A younger sister of the patient also has tyrosinemia and low hepatic tyrosine aminotransferase activity. 6147810 1984
CUI: C0268483
Disease: Tyrosinemias
Tyrosinemias 		0.420 Biomarker disease HPO
CUI: C0268483
Disease: Tyrosinemias
Tyrosinemias 		0.420 Biomarker disease CTD_human