MIR122, microRNA 122, 406906

N. diseases: 250; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266258
Disease: Congenital absence of liver
Congenital absence of liver
0.010 AlteredExpression disease BEFREE Fabp3 and Myl3 outperformed CK for detection of myofiber degeneration of minimal severity. miR-122 and ARG1 results were significantly correlated and indicated the absence of liver toxicity at low doses of clofibrate, despite increased ALT/AST activities. 28485676 2017