783250007: Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia\Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia\Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
• \Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia\Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
• \Disease\Congenital disease\Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3758276014	Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3758277017	Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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