TXN2, thioredoxin 2, 25828

N. diseases: 76; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3279904
Disease: Lactate Dehydrogenase B Deficiency
Lactate Dehydrogenase B Deficiency
0.010 Biomarker disease BEFREE Parkinson's disease, triosephosphate isomerase deficiency, combined oxidative phosphorylation deficiency, and lactate dehydrogenase b deficiency are some of the diseases where the proposed mitochondrial network of Trx2 may be implicated. 31018154 2019