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RGD ID: 735997
Species: Homo sapiens
RGD Object: Gene
Symbol: MSX2
Name: msh homeobox 2
Acc ID: DOID:2340
Term: craniosynostosis
Definition: A synostosis that results_in premature fusion located_in skull. (DO)
Definition Source(s): "DO" "DO", "DO" "DO", "DO" "DO", "DO" "DO"
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 1600491RGDcraniosynostosis type 2, OMIM:604757, DNA:point mutation:exon:P148H 
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