Gene: LAMB2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.220 Biomarker disease LHGDN A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2. 16921188 2006
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.220 Biomarker disease LHGDN Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities. 15367484 2004
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.220 Biomarker disease MGD