80387009: Roger's disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Cardiac finding\Heart disease\...

\Disorder of cardiac ventricle\Congenital abnormality of cardiac ventricle\Congenital ventricular septal defect\Roger's disease
\Disorder of cardiac ventricle\Ventricular septal abnormality\Ventricular septal defect\Congenital ventricular septal defect\Roger's disease

\Structural disorder of heart\Ventricular septal abnormality\Ventricular septal defect\Congenital ventricular septal defect\Roger's disease
\Structural disorder of heart\Cardiac septal defects\Congenital septal defect of heart\Congenital ventricular septal defect\Roger's disease
\Structural disorder of heart\Cardiac septal defects\Ventricular septal defect\Congenital ventricular septal defect\Roger's disease
\Structural disorder of heart\Congenital heart disease\Congenital anomaly of cardiac chamber\Congenital abnormality of cardiac ventricle\Congenital ventricular septal defect\Roger's disease
\Structural disorder of heart\Congenital heart disease\Congenital septal defect of heart\Congenital ventricular septal defect\Roger's disease

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

133392011 Roger's disease en Synonym Active Entire term case sensitive SNOMED CT core module

133393018 Asymptomatic ventricular septal defect en Synonym Active Entire term case insensitive SNOMED CT core module

504412011 Maladie de Roger en Synonym Active Entire term case sensitive SNOMED CT core module

504413018 Small ventricular septal defect en Synonym Active Entire term case insensitive SNOMED CT core module

821541014 Roger's disease (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

2840226015 Roger disease en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Roger's disease	Is a	Ventricular septal defect	false	Inferred relationship	Existential restriction modifier
Roger's disease	Finding site	Interventricular septum structure	true	Inferred relationship	Existential restriction modifier	1
Roger's disease	Associated morphology	Defect	false	Inferred relationship	Existential restriction modifier
Roger's disease	Associated morphology	Congenital abnormal communication	false	Inferred relationship	Existential restriction modifier	15
Roger's disease	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Roger's disease	Associated morphology	Congenital incomplete closure	false	Inferred relationship	Existential restriction modifier	1
Roger's disease	Finding site	Interventricular septum structure	false	Inferred relationship	Existential restriction modifier	1
Roger's disease	Associated morphology	Congenital abnormal communication	false	Inferred relationship	Existential restriction modifier	2
Roger's disease	Finding site	Interventricular septum structure	false	Inferred relationship	Existential restriction modifier	2
Roger's disease	Associated morphology	Congenital septal defect	false	Inferred relationship	Existential restriction modifier	1
Roger's disease	Is a	Congenital malformation	false	Inferred relationship	Existential restriction modifier
Roger's disease	Is a	Congenital heart disease	false	Inferred relationship	Existential restriction modifier
Roger's disease	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier
Roger's disease	Is a	Congenital anomaly of cardiovascular system	false	Inferred relationship	Existential restriction modifier
Roger's disease	Associated morphology	Congenital septal defect	false	Inferred relationship	Existential restriction modifier	1
Roger's disease	Finding site	Interventricular septum structure	false	Inferred relationship	Existential restriction modifier	1
Roger's disease	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Roger's disease	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Roger's disease	Finding site	Interventricular septum structure	false	Inferred relationship	Existential restriction modifier	2
Roger's disease	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Roger's disease	Associated morphology	Congenital failure of fusion	false	Inferred relationship	Existential restriction modifier	3
Roger's disease	Finding site	Interventricular septum structure	false	Inferred relationship	Existential restriction modifier	3
Roger's disease	Associated morphology	Developmental failure of fusion	false	Inferred relationship	Existential restriction modifier	2
Roger's disease	Is a	Congenital ventricular septal defect	true	Inferred relationship	Existential restriction modifier
Roger's disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Roger's disease	Associated morphology	Developmental failure of fusion	true	Inferred relationship	Existential restriction modifier	1
Roger's disease	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
133392011	Roger's disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
133393018	Asymptomatic ventricular septal defect	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
504412011	Maladie de Roger	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
504413018	Small ventricular septal defect	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
821541014	Roger's disease (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
2840226015	Roger disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module