Compare GO annotations related to Cornelia de Lange syndrome using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Cellular ComponentGO:0032116cohesin loading complex S000002588IPIYeastSGD_REF:S000060398|PMID:10882066
Biological ProcessGO:0000724double-strand break repair via homologous recombination S000002588IMPYeastSGD_REF:S000080735|PMID:15610742
Biological ProcessGO:0009792embryonic development ending in birth or egg hatching WBGene00004166IMPWormWB:WBPaper00005654|PMID:12529635
Biological ProcessGO:0009792embryonic development ending in birth or egg hatching WBGene00004166IMPWormWB:WBPaper00024497|PMID:15489339
Biological ProcessGO:0009792embryonic development ending in birth or egg hatching WBGene00004166IMPWormWB:WBPaper00025054|PMID:15791247
Biological ProcessGO:0009792embryonic development ending in birth or egg hatching WBGene00004166IMPWormWB:WBPaper00027710|PMID:16802858
Biological ProcessGO:0007626locomotory behavior WBGene00004166IMPWormWB:WBPaper00005654|PMID:12529635
Biological ProcessGO:0007064mitotic sister chromatid cohesion S000002588IMPYeastSGD_REF:S000054345|PMID:9335333
Biological ProcessGO:0040032post-embryonic body morphogenesis WBGene00004166IMPWormWB:WBPaper00005654|PMID:12529635