35728003: Familial cardiomyopathy (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Cardiac finding\...

\Myocardial finding\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy

\Heart disease\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy

\Finding of trunk structure\Finding of upper trunk (finding)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disorder of mediastinum (disorder)\Heart disease\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy
\Finding of trunk structure\Finding of upper trunk (finding)\Finding of region of thorax\Mediastinal finding (finding)\Cardiac finding\Myocardial finding\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy
\Finding of trunk structure\Finding of upper trunk (finding)\Finding of region of thorax\Mediastinal finding (finding)\Cardiac finding\Heart disease\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy
\Finding of trunk structure\Finding of upper trunk (finding)\Finding of region of thorax\Mediastinal finding (finding)\Disorder of mediastinum (disorder)\Heart disease\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy
\Finding of trunk structure\Finding of upper trunk (finding)\Finding of region of thorax\Disorder of thorax (disorder)\Disorder of mediastinum (disorder)\Heart disease\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disorder of mediastinum (disorder)\Heart disease\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy

\Cardiovascular finding\Cardiac finding\Myocardial finding\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy
\Cardiovascular finding\Cardiac finding\Heart disease\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy
\Cardiovascular finding\Disorder of cardiovascular system\Heart disease\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy

\Disease\Disorder of body system\Disorder of cardiovascular system\Heart disease\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy
\Disease\Disorder of body system\Disorder of mediastinum (disorder)\Heart disease\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy
\Disease\Disorder of trunk (disorder)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disorder of mediastinum (disorder)\Heart disease\Myocardial disease (disorder)\Cardiomyopathy (disorder)\Familial cardiomyopathy
\Disease\Familial disease\Familial cardiomyopathy

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial cardiomyopathy	Is a	Familial disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial cardiomyopathy	Is a	Primary cardiomyopathy	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial cardiomyopathy	Is a	Cardiovascular system hereditary disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial cardiomyopathy	Finding site	Myocardium structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial cardiomyopathy	Is a	Cardiomyopathy (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Danish type familial amyloid cardiomyopathy	Is a	True	Familial cardiomyopathy	Inferred relationship	Existential restriction modifier (core metadata concept)
Restrictive cardiomyopathy secondary to familial storage disease	Is a	False	Familial cardiomyopathy	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary familial dilated cardiomyopathy	Is a	False	Familial cardiomyopathy	Inferred relationship	Existential restriction modifier (core metadata concept)
Dilated cardiomyopathy due to familial storage disease (disorder)	Is a	False	Familial cardiomyopathy	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary familial hypertrophic cardiomyopathy (disorder)	Is a	True	Familial cardiomyopathy	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial restrictive cardiomyopathy (disorder)	Is a	True	Familial cardiomyopathy	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary familial dilated cardiomyopathy	Is a	True	Familial cardiomyopathy	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder)	Is a	True	Familial cardiomyopathy	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
59588016	Familial cardiomyopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
59589012	Primary familial cardiomyopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
767399015	Familial cardiomyopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
59588016	Familial cardiomyopathy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
59588016	Familial cardiomyopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
59589012	Primary familial cardiomyopathy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
59589012	Primary familial cardiomyopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
767399015	Familial cardiomyopathy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
767399015	Familial cardiomyopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
66571000077115	cardiomyopathie familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
66571000077115	cardiomyopathie familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module