EMP2, epithelial membrane protein 2, 2013

N. diseases: 46; N. variants: 5
Disease: NEPHROTIC SYNDROME, TYPE 10 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4014507
Disease: NEPHROTIC SYNDROME, TYPE 10
NEPHROTIC SYNDROME, TYPE 10 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in EMP2 cause childhood-onset nephrotic syndrome. 24814193 2014
CUI: C4014507
Disease: NEPHROTIC SYNDROME, TYPE 10
NEPHROTIC SYNDROME, TYPE 10 		0.700 GeneticVariation disease UNIPROT Mutations in EMP2 cause childhood-onset nephrotic syndrome. 24814193 2014
CUI: C4014507
Disease: NEPHROTIC SYNDROME, TYPE 10
NEPHROTIC SYNDROME, TYPE 10 		0.700 Biomarker disease CTD_human
CUI: C4014507
Disease: NEPHROTIC SYNDROME, TYPE 10
NEPHROTIC SYNDROME, TYPE 10 		0.700 CausalMutation disease CLINVAR