Disease: NEPHROTIC SYNDROME, TYPE 15 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4539896
Disease: NEPHROTIC SYNDROME, TYPE 15
NEPHROTIC SYNDROME, TYPE 15 		0.400 Biomarker disease GENOMICS_ENGLAND Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment. 29773874 2018
CUI: C4539896
Disease: NEPHROTIC SYNDROME, TYPE 15
NEPHROTIC SYNDROME, TYPE 15 		0.400 Biomarker disease GENOMICS_ENGLAND MAGI2 Mutations Cause Congenital Nephrotic Syndrome. 27932480 2017
CUI: C4539896
Disease: NEPHROTIC SYNDROME, TYPE 15
NEPHROTIC SYNDROME, TYPE 15 		0.400 Biomarker disease GENOMICS_ENGLAND MAGI-2 scaffold protein is critical for kidney barrier function. 25271328 2014
CUI: C4539896
Disease: NEPHROTIC SYNDROME, TYPE 15
NEPHROTIC SYNDROME, TYPE 15 		0.400 CausalMutation disease CLINVAR