Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1749
Gene Symbol: DLX5
DLX5
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.310 Biomarker CTD_human Dlx5/6-enhancer directed expression of Cre recombinase in the pharyngeal arches and brain. 14666512

2003
Entrez Id: 1749
Gene Symbol: DLX5
DLX5
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.310 Biomarker CTD_human Dlx5 regulates regional development of the branchial arches and sensory capsules. 10433912

1999
Entrez Id: 1749
Gene Symbol: DLX5
DLX5
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.310 Biomarker CTD_human Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5. 10433909

1999