33169001: Factor XI deficiency, type II (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\...
• \Contact factor deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
• \Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
• \Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Contact factor deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
• \Disease\Congenital disease\Hereditary factor XI deficiency disease\Factor XI deficiency, type II

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
55354017	Factor XI deficiency, type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
764538019	Factor XI deficiency, type II (disorder)	en	Fully specified name	Active	Initial character case insensitive	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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