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766883006: Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3663008016 Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3663009012 Familial dilated cardiomyopathy with conduction defect due to LMNA mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3663010019 Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5404694016 A rare familial cardiomyopathy characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404695015 A rare familial cardiomyopathy characterised by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3663008016 Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3663009012 Familial dilated cardiomyopathy with conduction defect due to LMNA mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3663010019 Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3663011015 A rare familial dilated cardiomyopathy with characteristics of left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy and elevated serum creatine kinase. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404694016 A rare familial cardiomyopathy characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404695015 A rare familial cardiomyopathy characterised by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3397581001000119 Familiäre dilatative Kardiomyopathie mit Reizleitungs-Defekt durch LMNA-Genmutation de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3397581001000119 Familiäre dilatative Kardiomyopathie mit Reizleitungs-Defekt durch LMNA-Genmutation de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) Finding site Myocardium structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) Finding site Cardiac conducting system structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) Is a Familial cardiomyopathy true Inferred relationship Existential restriction modifier (core metadata concept)
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) Is a Congestive cardiomyopathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) Associated morphology Dilatation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) Is a Conduction disorder of the heart true Inferred relationship Existential restriction modifier (core metadata concept)
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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