DLX2, distal-less homeobox 2, 1746

N. diseases: 34; N. variants: 2
Disease: AL-RAQAD SYNDROME ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4085595
Disease: AL-RAQAD SYNDROME
AL-RAQAD SYNDROME 		0.020 AlteredExpression disease BEFREE Gene expression profiling of homozygous Pitx2 mutant mouse tissue reveals decreased Dlx2 expression as a potential molecular basis for developmental defects associated with ARS patients. 15751970 2005
CUI: C4085595
Disease: AL-RAQAD SYNDROME
AL-RAQAD SYNDROME 		0.020 AlteredExpression disease BEFREE Altogether these data suggest a molecular mechanism for tooth development involving Dlx2 gene expression in ARS patients. 11929847 2002