715559004: Combined deficiency of factor V and factor VIII (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...
• \Combined coagulation factor deficiency\Hereditary combined coagulation factor deficiency\Combined deficiency of factor V and factor VIII
• \Factor VIII deficiency\Combined deficiency of factor V and factor VIII
• \Hereditary coagulation factor deficiency\Hereditary combined coagulation factor deficiency\Combined deficiency of factor V and factor VIII
• \Factor V deficiency\Combined deficiency of factor V and factor VIII
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary combined coagulation factor deficiency\Combined deficiency of factor V and factor VIII
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined deficiency of factor V and factor VIII
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Combined coagulation factor deficiency\Hereditary combined coagulation factor deficiency\Combined deficiency of factor V and factor VIII
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor VIII deficiency\Combined deficiency of factor V and factor VIII
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary combined coagulation factor deficiency\Combined deficiency of factor V and factor VIII
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor V deficiency\Combined deficiency of factor V and factor VIII

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3303019018	Combined deficiency of factor V and factor VIII (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3303020012	Combined deficiency of factor V and factor VIII	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3303021011	Factor V and factor VIII combined deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3303022016	Familial multiple coagulation factor deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3303023014	An inherited bleeding disorder caused by the reduction in activity and antigen levels of both factor V and factor VIII with manifestation of mild-to-moderate bleeding symptoms. Caused by mutations either in the LMAN1 gene (chromosome 18; q21) or in the MCFD2 gene (chromosome 2). Transmission is autosomal recessive.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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