EMX2, empty spiracles homeobox 2, 2018

N. diseases: 59; N. variants: 2
Disease: Familial schizencephaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931870
Disease: Familial schizencephaly
Familial schizencephaly 		0.320 Biomarker disease BEFREE EMX2-independent familial schizencephaly: clinical and genetic analyses. 15887302 2005
CUI: C2931870
Disease: Familial schizencephaly
Familial schizencephaly 		0.320 GeneticVariation disease BEFREE Familial schizencephaly associated with EMX2 mutation. 9153481 1997
CUI: C2931870
Disease: Familial schizencephaly
Familial schizencephaly 		0.320 Biomarker disease CTD_human