724356003: Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...
• \Combined coagulation factor deficiency\Hereditary combined coagulation factor deficiency (disorder)\Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)
• \Hereditary coagulation factor deficiency\Hereditary combined coagulation factor deficiency (disorder)\Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary combined coagulation factor deficiency (disorder)\Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Inborn error of metabolism\Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Combined coagulation factor deficiency\Hereditary combined coagulation factor deficiency (disorder)\Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary combined coagulation factor deficiency (disorder)\Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3434469011	Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3434470012	Hereditary combined deficiency of vitamin K-dependent clotting factors	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3434471011	Hereditary combined deficiency of factors II, VII, IX and X	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5403316015	Combined vitamin K-dependent clotting factors deficiency (VKCFD) is a congenital bleeding disorder resulting from variably decreased levels of coagulation factors II, VII, IX and X, as well as natural anticoagulants protein C, protein S and protein Z.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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