LAMA3, laminin subunit alpha 3, 3909

N. diseases: 110; N. variants: 86
Disease: Abnormality of dental enamel ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel 		0.010 GeneticVariation group BEFREE The reported enamel abnormality in LAMA3 mutation carriers could be attributed to a half dose effect of the laminin α3 chain (haploinsufficiency). 27827380 2016