725291001: Defect of purinergic receptor p2y G protein-coupled 12 (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\...
• \Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Functional finding\Disorder of hemostatic system\...
• \Blood coagulation disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Disease\Disorder of cellular component of blood\Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Disease\Disorder of cellular component of blood\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Disease\Disorder of hemostatic system\Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Disease\Disorder of hemostatic system\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Defect of purinergic receptor p2y G protein-coupled 12
• \Disease\Congenital disease\Defect of purinergic receptor p2y G protein-coupled 12

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
3440815011	Defect of purinergic receptor p2y G protein-coupled 12 (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3440816012	Defect of purinergic receptor p2y G protein-coupled 12	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3440817015	ADP platelet receptor P2Y12 defect	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3440818013	P2Y12 (purinergic receptor p2y G protein-coupled 12) defect	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3440819017	P2Y12 defect	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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