HMX1, H6 family homeobox 1, 3166

N. diseases: 23; N. variants: 1
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 Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass. 19379485 2009