1162804003: Hereditary congenital prekallikrein deficiency (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Disorder of hemostatic system\Blood coagulation disorder\...
• \Contact factor deficiency\Prekallikrein deficiency\Hereditary congenital prekallikrein deficiency (disorder)
• \Coagulation factor deficiency syndrome\Prekallikrein deficiency\Hereditary congenital prekallikrein deficiency (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary congenital prekallikrein deficiency (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary congenital prekallikrein deficiency (disorder)
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Contact factor deficiency\Prekallikrein deficiency\Hereditary congenital prekallikrein deficiency (disorder)
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Prekallikrein deficiency\Hereditary congenital prekallikrein deficiency (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4591510019	Hereditary congenital prekallikrein deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4591511015	Hereditary congenital prekallikrein deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4591518014	Congenital Fletcher factor deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4591514011	A rare genetic coagulation disorder characterised by the usually incidental laboratory finding of a prolonged activated partial thromboplastin time (aPTT) but normal prothrombin time, due to a deficiency of normal prekallikrein or the presence of nonfunctional prekallikrein. Most patients remain clinically asymptomatic, although an association with cardiovascular conditions (hypertension, myocardial infarction, other coronary artery diseases, and ischaemic strokes) and venous thrombosis, as well as rare cases with increased bleeding tendency have been reported.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4591515012	A rare genetic coagulation disorder characterized by the usually incidental laboratory finding of a prolonged activated partial thromboplastin time (aPTT) but normal prothrombin time, due to a deficiency of normal prekallikrein or the presence of nonfunctional prekallikrein. Most patients remain clinically asymptomatic, although an association with cardiovascular conditions (hypertension, myocardial infarction, other coronary artery diseases, and ischemic strokes) and venous thrombosis, as well as rare cases with increased bleeding tendency have been reported.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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