Compare GO annotations related to Ectodermal dysplasia, hypohidrotic, autosomal dominant using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0005515protein binding Q9UNE0IPIHumanPMID:11035039
Cellular ComponentGO:0045177apical part of cell MGI:1343498IDAMouseMGI:MGI:3617077|PMID:12629675
Cellular ComponentGO:0005886plasma membrane MGI:1343498IDAMouseMGI:MGI:3617077|PMID:12629675
Biological ProcessGO:0001942hair follicle development MGI:1343498IMPMouseMGI:MGI:54784|PMID:544312
Biological ProcessGO:0001942hair follicle development MGI:1343498IGIMouseMGI:MGI:54784|PMID:544312
Biological ProcessGO:0042475odontogenesis of dentine-containing teeth MGI:1343498IMPMouseMGI:MGI:54784|PMID:544312
Biological ProcessGO:0043473pigmentation MGI:1343498IMPMouseMGI:MGI:54784|PMID:544312
Biological ProcessGO:0042346positive regulation of NF-kappaB import into nucleus MGI:1343498IDAMouseMGI:MGI:3617077|PMID:12629675
Biological ProcessGO:0007431salivary gland development MGI:1343498IDAMouseMGI:MGI:3617077|PMID:12629675