GTF2IRD1, GTF2I repeat domain containing 1, 9569

N. diseases: 222; N. variants: 8
Disease: Craniofacial Abnormalities ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.310 Biomarker group CTD_human Mice with mutations of the Gtf2ird1 allele show evidence of craniofacial abnormalities and behavioral changes. 20007321 2010
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.310 GeneticVariation group BEFREE Mice with mutations of the Gtf2ird1 allele show evidence of craniofacial abnormalities and behavioral changes. 20007321 2010