88540000: Factor XI deficiency, type I (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 I
• \Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type I
• \Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor XI deficiency disease\Factor XI deficiency, type I
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary factor XI deficiency disease\Factor XI deficiency, type I
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Contact factor deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type I
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type I
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor XI deficiency disease\Factor XI deficiency, type I
• \Disease\Congenital disease\Hereditary factor XI deficiency disease\Factor XI deficiency, type I

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
146804016	Factor XI deficiency, type I	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
831245011	Factor XI deficiency, type I (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

Back to Start