OTX2, orthodenticle homeobox 2, 5015

N. diseases: 200; N. variants: 23
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0022360
Disease: Jaw Abnormalities
Jaw Abnormalities
0.300 Biomarker group CTD_human Genetic modifiers of otocephalic phenotypes in Otx2 heterozygous mutant mice. 12183386 2002