FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  FHIR Version n/a  User: [n/a]

35728003: Familial cardiomyopathy (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
59588016 Familial cardiomyopathy en Synonym Active Entire term case insensitive SNOMED CT core module
59589012 Primary familial cardiomyopathy en Synonym Active Entire term case insensitive SNOMED CT core module
767399015 Familial cardiomyopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

8 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial cardiomyopathy Is a Familial disease true Inferred relationship Existential restriction modifier
Familial cardiomyopathy Is a Primary cardiomyopathy false Inferred relationship Existential restriction modifier
Familial cardiomyopathy Is a Cardiovascular system hereditary disorder false Inferred relationship Existential restriction modifier
Familial cardiomyopathy Finding site Myocardium structure true Inferred relationship Existential restriction modifier 1
Familial cardiomyopathy Is a Cardiomyopathy true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Danish type familial amyloid cardiomyopathy Is a True Familial cardiomyopathy Inferred relationship Existential restriction modifier
Restrictive cardiomyopathy secondary to familial storage disease Is a False Familial cardiomyopathy Inferred relationship Existential restriction modifier
Primary familial dilated cardiomyopathy Is a False Familial cardiomyopathy Inferred relationship Existential restriction modifier
Dilated cardiomyopathy due to familial storage disease Is a False Familial cardiomyopathy Inferred relationship Existential restriction modifier
Primary familial hypertrophic cardiomyopathy Is a True Familial cardiomyopathy Inferred relationship Existential restriction modifier
Familial restrictive cardiomyopathy Is a True Familial cardiomyopathy Inferred relationship Existential restriction modifier
Primary familial dilated cardiomyopathy Is a True Familial cardiomyopathy Inferred relationship Existential restriction modifier
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation Is a True Familial cardiomyopathy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start