Disease: Proteinuria ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0033687
Disease: Proteinuria
Proteinuria 		0.400 Biomarker phenotype GENOMICS_ENGLAND Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy. 25165188 2014
CUI: C0033687
Disease: Proteinuria
Proteinuria 		0.400 GeneticVariation phenotype CLINVAR
CUI: C0033687
Disease: Proteinuria
Proteinuria 		0.400 Biomarker phenotype HPO