LAMB2, laminin subunit beta 2, 3913

N. diseases: 116; N. variants: 17
Disease: Sclerosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036429
Disease: Sclerosis
Sclerosis 		0.010 Biomarker phenotype LHGDN Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities. 15367484 2004