DLX3, distal-less homeobox 3, 1747

N. diseases: 67; N. variants: 5
Disease: Taurodontism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266039
Disease: Taurodontism
Taurodontism 		0.140 GeneticVariation disease BEFREE Previously, the DLX3 c.561_562delCT mutation was associated with autosomal dominant amelogenesis imperfecta with taurodontism. 18203197 2008
CUI: C0266039
Disease: Taurodontism
Taurodontism 		0.140 GeneticVariation disease BEFREE Recently, another DLX3 gene mutation (c.561_562delCT) was reported to cause amelogenesis imperfecta with taurodontism (AIHHT). 18362318 2008
CUI: C0266039
Disease: Taurodontism
Taurodontism 		0.140 Biomarker disease BEFREE Late genes expressed during root formation (ALPL and DLX3) are associated with cementum agenesis (hypophosphatasia) and taurodontism. 17552940 2007
CUI: C0266039
Disease: Taurodontism
Taurodontism 		0.140 GeneticVariation disease BEFREE DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism. 15666299 2005
CUI: C0266039
Disease: Taurodontism
Taurodontism 		0.140 Biomarker disease HPO
CUI: C0266039
Disease: Taurodontism
Taurodontism 		0.140 CausalMutation disease CLINVAR