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35728003: Familial cardiomyopathy (disorder)


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

Descriptions:

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
66571000077115 cardiomyopathie familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
688741000077110 cardiomyopathie familiale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
767399015 Familial cardiomyopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


8 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial cardiomyopathy est un(e) (attribut) Familial disease true Inferred relationship Some
Familial cardiomyopathy est un(e) (attribut) Primary cardiomyopathy false Inferred relationship Some
Familial cardiomyopathy est un(e) (attribut) Cardiovascular system hereditary disorder false Inferred relationship Some
Familial cardiomyopathy est un(e) (attribut) Cardiomyopathy true Inferred relationship Some
Familial cardiomyopathy localisation d'une constatation (attribut) structure du myocarde true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Danish type familial amyloid cardiomyopathy est un(e) (attribut) True Familial cardiomyopathy Inferred relationship Some
Familial restrictive cardiomyopathy est un(e) (attribut) True Familial cardiomyopathy Inferred relationship Some
Restrictive cardiomyopathy secondary to familial storage disease est un(e) (attribut) False Familial cardiomyopathy Inferred relationship Some
Primary familial dilated cardiomyopathy (disorder) est un(e) (attribut) False Familial cardiomyopathy Inferred relationship Some
Dilated cardiomyopathy due to familial storage disease (disorder) est un(e) (attribut) False Familial cardiomyopathy Inferred relationship Some
Primary familial hypertrophic cardiomyopathy est un(e) (attribut) True Familial cardiomyopathy Inferred relationship Some
Primary familial dilated cardiomyopathy (disorder) est un(e) (attribut) True Familial cardiomyopathy Inferred relationship Some
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation est un(e) (attribut) True Familial cardiomyopathy Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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