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