HOXA3, homeobox A3, 3200

N. diseases: 36; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities
0.300 Biomarker group CTD_human Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5. 1673020 1991