|
MIM:610293 - GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 1; GPIBD1
Xenbase Genes: pigm
Human Disease Resource: OMIM
MONDO:0012465 - hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency |
|
MONDO:0012465 - hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency |