LAMB2, laminin subunit beta 2, 3913

N. diseases: 116; N. variants: 17
Disease: Low Vision ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0042798
Disease: Low Vision
Low Vision 		0.010 GeneticVariation disease BEFREE A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2. 16921188 2006