MSX2, msh homeobox 2, 4488

N. diseases: 135; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018681
Disease: Headache
Headache
0.110 GeneticVariation phenotype LHGDN A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly. 16642368 2006
CUI: C0018681
Disease: Headache
Headache
0.110 Biomarker phenotype HPO