Compare GO annotations related to Lipodystrophy, congenital generalized, type 2 using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Cellular ComponentGO:0030176integral to endoplasmic reticulum membrane Q96G97IDAHumanPMID:14981520