LAMB2, laminin subunit beta 2, 3913

N. diseases: 116; N. variants: 17
Disease: Familial mesangial sclerosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3489732
Disease: Familial mesangial sclerosis
Familial mesangial sclerosis 		0.300 Biomarker phenotype CTD_human Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities. 15367484 2004