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442917000: Familial long QT syndrome (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2837534014 Congenital long QT syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2837535010 Inherited long QT syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3901309016 Familial long QT syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5223382019 Familial long QT syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5223383012 A rare group of genetic, cardiac rhythm diseases with characteristics of a prolongation of the QT interval at basal electrocardiography (ECG) and by a high risk of life-threatening arrhythmias. The two cardinal manifestations are syncopal episodes, which may lead to cardiac arrest and sudden cardiac death, and electrocardiographic abnormalities: prolongation of the QT interval and T wave abnormalities. Inheritance may be autosomal dominant or autosomal recessive and depends on the genes involved. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
2834302013 Congenital long QT syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2837534014 Congenital long QT syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2837535010 Inherited long QT syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3901309016 Familial long QT syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5223382019 Familial long QT syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5223383012 A rare group of genetic, cardiac rhythm diseases with characteristics of a prolongation of the QT interval at basal electrocardiography (ECG) and by a high risk of life-threatening arrhythmias. The two cardinal manifestations are syncopal episodes, which may lead to cardiac arrest and sudden cardiac death, and electrocardiographic abnormalities: prolongation of the QT interval and T wave abnormalities. Inheritance may be autosomal dominant or autosomal recessive and depends on the genes involved. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3382301001000115 Long-QT-Syndrom, familiäres de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6969321000241113 syndrome du QT long congénital fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6969331000241110 syndrome du QT long familial fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6969321000241113 syndrome du QT long congénital fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6969331000241110 syndrome du QT long familial fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3382301001000115 Long-QT-Syndrom, familiäres de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

15 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial long QT syndrome Is a Long QT syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Familial long QT syndrome Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
Familial long QT syndrome Finding site Cardiac conducting system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Familial long QT syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial long QT syndrome Finding site Heart structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Familial long QT syndrome Is a A disorder in which there is abnormal electrical activity in the heart associated with a genetic disorder. true Inferred relationship Existential restriction modifier (core metadata concept)
Familial long QT syndrome Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Familial long QT syndrome Is a Congenital cardiovascular disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial long QT syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Familial long QT syndrome Finding site Heart structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial long QT syndrome Finding site Cardiac conducting system structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Romano-Ward syndrome (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Long QT syndrome with genetic marker Is a False Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Andersen Tawil syndrome Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Timothy syndrome type 2 (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Timothy syndrome type 1 Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Long QT syndrome type 9 (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Long QT syndrome type 6 (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Family history of congenital long QT syndrome Associated finding True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept) 1
Long QT syndrome type 4 (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Long QT syndrome type 5 (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Long QT syndrome type 2 (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Long QT syndrome type 11 (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Long QT syndrome type 10 (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Long QT syndrome type 3 (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Long QT syndrome type 12 (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Long QT syndrome type 13 (disorder) Is a True Familial long QT syndrome Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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