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80387009: Roger's disease (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Roger's disease Occurrence Congenital true Inferred relationship Some 1
Roger's disease Associated morphology Developmental failure of fusion true Inferred relationship Some 1
Roger's disease Pathological process Pathological developmental process true 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 false Inferred relationship Some 1
Roger's disease Is a Congenital anomaly 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 Is a Ventricular septal defect false Inferred relationship Some
Roger's disease Associated morphology Congenital septal defect 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 abnormality 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 false Inferred relationship Some 2
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 Is a Congenital ventricular septal defect true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

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