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)\anomalie du septum interventriculaire\Ventricular septal defect\Congenital ventricular septal defect\Roger's disease

\Structural disorder of heart\anomalie du septum interventriculaire\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 (disorder)\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 (disorder)\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	Existential restriction modifier (core metadata concept)
Roger's disease	Finding site	Interventricular septum structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Roger's disease	Associated morphology	Defect	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Roger's disease	Associated morphology	Congenital abnormal communication	false	Inferred relationship	Existential restriction modifier (core metadata concept)	15
Roger's disease	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Roger's disease	Associated morphology	Congenital incomplete closure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Roger's disease	Finding site	Interventricular septum structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Roger's disease	Associated morphology	Congenital abnormal communication	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Roger's disease	Finding site	Interventricular septum structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Roger's disease	Associated morphology	Congenital septal defect	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Roger's disease	Is a	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Roger's disease	Is a	Congenital heart disease (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Roger's disease	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Roger's disease	Is a	Congenital anomaly of cardiovascular system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Roger's disease	Associated morphology	Congenital septal defect	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Roger's disease	Finding site	Interventricular septum structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Roger's disease	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Roger's disease	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Roger's disease	Finding site	Interventricular septum structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Roger's disease	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Roger's disease	Associated morphology	Congenital failure of fusion	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Roger's disease	Finding site	Interventricular septum structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Roger's disease	Associated morphology	Developmental failure of fusion (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Roger's disease	Is a	Congenital ventricular septal defect	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Roger's disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Roger's disease	Associated morphology	Developmental failure of fusion (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Roger's disease	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Roger's disease	Associated morphology	Abnormal communication (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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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
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	Only initial character case insensitive (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	Only initial character case insensitive (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	Only initial character 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
4653191000241111	maladie de Roger	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4653191000241111	maladie de Roger	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module