MSX2, msh homeobox 2, 4488

N. diseases: 135; N. variants: 7
Disease: Familial hypodontia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1290514
Disease: Familial hypodontia
Familial hypodontia 		0.010 GeneticVariation disease BEFREE Here, we studied the relationship of the MSX1 and MSX2 genes to familial hypodontia in five Finnish families with a total of 20 affected individuals, by linkage analysis. 7649547 1995