80387009: Roger's disease (disorder)

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

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

\Disorder of cardiac ventricle (disorder)\Congenital abnormality of cardiac ventricle\Congenital ventricular septal defect\Roger's disease
\Disorder of cardiac ventricle (disorder)\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 (disorder)\Congenital abnormality of cardiac ventricle\Congenital ventricular septal defect\Roger's disease
\Structural disorder of heart\Congenital heart disease\Congenital abnormality of cardiac connection\Congenital septal defect of heart\Congenital ventricular septal defect\Roger's disease

Status: current, Not 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
Roger's disease	Is a	Ventricular septal defect	false	Inferred relationship	Some
Roger's disease	Finding site	Interventricular septum structure	true	Inferred relationship	Some	1
Roger's disease	Associated morphology	defect	false	Inferred relationship	Some
Roger's disease	Associated morphology	Congenital abnormal communication	false	Inferred relationship	Some	15
Roger's disease	Occurrence	Congenital	false	Inferred relationship	Some
Roger's disease	Associated morphology	Congenital incomplete closure	false	Inferred relationship	Some	1
Roger's disease	Finding site	Interventricular septum structure	false	Inferred relationship	Some	1
Roger's disease	Associated morphology	Congenital abnormal communication	false	Inferred relationship	Some	2
Roger's disease	Finding site	Interventricular septum structure	false	Inferred relationship	Some	2
Roger's disease	Associated morphology	Congenital septal defect (morphologic abnormality)	false	Inferred relationship	Some	1
Roger's disease	Is a	Congenital malformation	false	Inferred relationship	Some
Roger's disease	Is a	Congenital heart disease	false	Inferred relationship	Some
Roger's disease	Is a	Congenital anomaly of trunk	false	Inferred relationship	Some
Roger's disease	Is a	Congenital anomaly of cardiovascular system	false	Inferred relationship	Some
Roger's disease	Associated morphology	Congenital septal defect (morphologic abnormality)	false	Inferred relationship	Some	1
Roger's disease	Finding site	Interventricular septum structure	false	Inferred relationship	Some	1
Roger's disease	Occurrence	Congenital	false	Inferred relationship	Some	2
Roger's disease	Associated morphology	Developmental anomaly	false	Inferred relationship	Some	2
Roger's disease	Finding site	Interventricular septum structure	false	Inferred relationship	Some	2
Roger's disease	Occurrence	Congenital	false	Inferred relationship	Some	3
Roger's disease	Associated morphology	Congenital failure of fusion	false	Inferred relationship	Some	3
Roger's disease	Finding site	Interventricular septum structure	false	Inferred relationship	Some	3
Roger's disease	Associated morphology	Developmental failure of fusion (morphologic abnormality)	false	Inferred relationship	Some	2
Roger's disease	Is a	Congenital ventricular septal defect	true	Inferred relationship	Some
Roger's disease	Occurrence	Congenital	true	Inferred relationship	Some	1
Roger's disease	Associated morphology	Developmental failure of fusion (morphologic abnormality)	false	Inferred relationship	Some	1
Roger's disease	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Roger's disease	Associated morphology	Abnormal communication	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Belgian GP subset (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
133392011	Roger's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
133393018	Asymptomatic ventricular septal defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
504412011	Maladie de Roger	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
504413018	Small ventricular septal defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
821541014	Roger's disease (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2840226015	Roger disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2118121000172112	maladie de Roger	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
2238541000172118	maladie congénitale de Roger	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
2118111000172119	ziekte van Roger	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
2238551000172116	congenitale ziekte van Roger	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)