Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type
0.200 Biomarker disease MGD Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout mice. 18818194 2009
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type
0.200 Biomarker disease MGD Course of renal injury in the Mpv17-deficient transgenic mouse. 10820170 2000
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type
0.200 Biomarker disease MGD Glomerular overproduction of oxygen radicals in Mpv17 gene-inactivated mice causes podocyte foot process flattening and proteinuria: A model of steroid-resistant nephrosis sensitive to radical scavenger therapy. 10233845 1999
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type
0.200 Biomarker disease MGD Age-dependent hypertension in Mpv17-deficient mice, a transgenic model of glomerulosclerosis and inner ear disease. 10673153 1999
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type
0.200 Biomarker disease MGD Functional rescue of the glomerulosclerosis phenotype in Mpv17 mice by transgenesis with the human Mpv17 homologue. 7564095 1995
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type
0.200 Biomarker disease MGD Transgenic mouse model of kidney disease: insertional inactivation of ubiquitously expressed gene leads to nephrotic syndrome. 1696177 1990