724344004: Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia\Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia\Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
• \Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia\Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
• \Disease\Congenital disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3434247018	Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3434248011	Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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