KMO, kynurenine 3-monooxygenase, 8564

N. diseases: 44; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
0.050 Biomarker disease BEFREE Kynurenine 3-monooxygenase (KMO) is a well-validated therapeutic target for the treatment of neurodegenerative diseases, including Alzheimer's disease (AD) and Huntington's disease (HD). 29420107 2018
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
0.050 Biomarker disease BEFREE Assessing and Modulating Kynurenine Pathway Dynamics in Huntington's Disease: Focus on Kynurenine 3-Monooxygenase. 29856028 2018
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
0.050 Biomarker disease BEFREE A number of inhibitors of kynurenine 3-monooxygenase (KMO) have previously been described as potential treatments for neurodegenerative conditions and particularly for Huntington's disease. 28398044 2017
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
0.050 Biomarker disease BEFREE BNA4 encodes the yeast homolog of kynurenine 3-monooxygenase, a promising drug target for HD. 21044956 2011
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
0.050 Biomarker disease BEFREE Among the most potent suppressors was Bna4 (kynurenine 3-monooxygenase), an enzyme in the kynurenine pathway of tryptophan degradation that has been linked directly to the pathophysiology of Huntington disease in humans by a mechanism that may involve reactive oxygen species. 15806102 2005