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RGD ID: 735997
Species: Homo sapiens
RGD Object: Gene
Symbol: MSX2
Name: msh homeobox 2
Acc ID: DOID:9008731
Term: Craniofacial Abnormalities
Definition: Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones.
Definition Source(s): MESH:D019465
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
MSX2 IAGP 1600492RGDparietal foramina, OMIM:168500, DNA:point mutation:exon: R172H, DNA:deletions 
MSX2 EXP 11554173CTDCTD Direct Evidence: marker/mechanismPMID:9147639
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