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


Status: current, Primitive. 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 Active Initial character case insensitive SNOMED CT core
3663009012 Familial dilated cardiomyopathy with conduction defect due to LMNA mutation en Synonym Active Initial character case insensitive SNOMED CT core
3663010019 Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) en Fully specified name Active Initial character case insensitive 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 Case sensitive SNOMED CT core


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 Finding site Myocardium structure true Inferred relationship Some 1
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation Finding site Cardiac conducting system structure true Inferred relationship Some 2
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation Is a Familial cardiomyopathy true Inferred relationship Some
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation Is a Congestive cardiomyopathy true Inferred relationship Some
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation Associated morphology Dilatation true Inferred relationship Some 1
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation Is a Conduction disorder of the heart true Inferred relationship Some
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation Is a Autosomal dominant hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

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