ERLIN2, ER lipid raft associated 2, 11160

N. diseases: 85; N. variants: 4
Disease: Primary lateral sclerosis juvenile ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1853396
Disease: Primary lateral sclerosis juvenile
Primary lateral sclerosis juvenile 		0.310 GermlineCausalMutation disease ORPHANET Loss of ERLIN2 function leads to juvenile primary lateral sclerosis. 23109145 2012
CUI: C1853396
Disease: Primary lateral sclerosis juvenile
Primary lateral sclerosis juvenile 		0.310 Biomarker disease BEFREE Loss of ERLIN2 function leads to juvenile primary lateral sclerosis. 23109145 2012