Compare GO annotations related to DiGeorge syndrome using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0042803protein homodimerization activity O43435IDAHumanPMID:11111039
Molecular FunctionGO:0043565sequence-specific DNA binding O43435IDAHumanPMID:11111039
Cellular ComponentGO:0005634nucleus O43435IDAHumanPMID:15703190
Biological ProcessGO:0048703embryonic viscerocranium morphogenesis O43435IMPHumanPMID:14585638
Biological ProcessGO:0007507heart development O43435IMPHumanPMID:14585638
Biological ProcessGO:0042694muscle cell fate specification WBGene00003376IMPWormWB:WBPaper00005080|PMID:11799068
Biological ProcessGO:0060017parathyroid gland development O43435IMPHumanPMID:14585638
Biological ProcessGO:0060037pharyngeal system development O43435IMPHumanPMID:14585638
Biological ProcessGO:0009791post-embryonic development WBGene00003376IMPWormWB:WBPaper00005080|PMID:11799068
Biological ProcessGO:0060023soft palate development O43435IMPHumanPMID:14585638
Biological ProcessGO:0048538thymus development O43435IMPHumanPMID:14585638