SOD1, superoxide dismutase 1, 6647

N. diseases: 689; N. variants: 68
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
0.070 Biomarker disease BEFREE Our study not only provides important proof-of-principle data for the development of a safe and effective human therapeutic/prophylactic ALS vaccine against misfolded SOD1, but also predicts a great potential to extend our DSE-based vaccination approach to other types of ALS, such as those associated with TDP-43 proteinopathies. 31324499 2019
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
0.070 Biomarker disease BEFREE More importantly, the early appearance of persistent pathological stress granules prior to significant pTDP-43 deposition implicates an aberrant stress granule response as a key disease mechanism driving TDP-43 proteinopathy in c9FTD/ALS. 30767771 2019
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
0.070 Biomarker disease BEFREE Microglia-mediated recovery from ALS-relevant motor neuron degeneration in a mouse model of TDP-43 proteinopathy. 29463850 2018
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
0.070 GeneticVariation disease BEFREE TDP-43 proteinopathy, initially associated with ALS and FTD, is also found in 30-60% of Alzheimer's disease (AD) cases and correlates with worsened cognition and neurodegeneration. 27785573 2016
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
0.070 Biomarker disease BEFREE The resulting elevation of the steady state level of hTDP-43 in combination with the relatively low tolerance of the spinal motor neurons to the increased amount of hTDP-43 lead to the neurodegeneration and pathogenesis of ALS, and of diseases with TDP-43 proteinopathies in general. 23721326 2013
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
0.070 GeneticVariation disease BEFREE The spectrum of TDP-43 proteinopathies includes FTLD-TDP with or without ALS, with or without mutations in GRN, VCP, or TARDBP, with or without chromosome 9p linkage, and sporadic and non-SOD1 familial ALS with or without FTLD-TDP. 21607722 2011
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
0.070 Biomarker disease BEFREE This unusual combination of inclusions appears pathognomonic for C9orf72 repeat expansion positive MND/ALS and FTLD-TDP which we believe form a pathologically distinct subset of TDP-43 proteinopathies. 22101323 2011